Radiation Safety Manual 2014

University of Illinois
at Urbana•Champaign
Radiation
Safety
Manual
Emergency reference information:
MetCAD………….……………………………...9-911
Radiation Safety….…………………………….3-2755
Spills or fires…………………………..………page 10
Revised: April 2014

Radiation Safety Manual
TABLE OF CONTENTS
1.0 Introduction ....................................................................................................................... 1

2.0 Authorization of Ionizing Radiation Sources ................................................................. 2
2.1 Radiation Permit Application Process ............................................................................ 2
2.2 Radiation Permit Validity ............................................................................................... 2
2.3 Amendments ................................................................................................................... 2
2.4 Deactivating/Reactivating a Permit ................................................................................ 3
2.5 Abandoned Radioactive Materials .................................................................................. 3
3.0 Radiation Safety Training Requirements ....................................................................... 4
4.0 Procurement and Transfer of Radioactive Materials.................................................... 5
4.1 Ordering Radioactive Materials ...................................................................................... 5
4.2 Receipt of Radioactive Materials .................................................................................... 5
4.3 On-Campus Transfers of Radioactive Materials............................................................. 6
4.4 Off-campus Transfers of Radioactive Materials ............................................................. 7
4.5 Transfers of Radioactive Materials from Off-campus .................................................... 7
5.0 Using Radioactive Materials ............................................................................................ 8
5.1 Storage of Radioactive Materials .................................................................................... 8
5.2 Using Radioisotopes in Animals ..................................................................................... 9
6.0 Emergency Procedures ................................................................................................... 10
6.1 Serious Injury and Exposure or Contamination ............................................................ 10
6.2 Fire or Explosion in a Radioisotope Area ..................................................................... 10
6.3 High Radiation Exposure Without Contamination ....................................................... 11
6.4 Intermediate and High-Level Radioactive Spills .......................................................... 11
7.0 Personnel Exposure ........................................................................................................ 13
7.1 Occupational Exposure Limits ...................................................................................... 13
7.2 Non-Occupational Exposure Limits (Members of the Public) ..................................... 13
7.3 Declared Pregnant Workers Exposure Limits............................................................... 13
7.4 Exposure Limits for Minors .......................................................................................... 14
7.5 When Dosimetry Is Required........................................................................................ 14
7.6 Bioassays....................................................................................................................... 14
7.7 Personnel Exposure Records......................................................................................... 15
7.8 ALARA (As Low As Reasonably Achievable) ............................................................ 15
7.9 Exposure Reduction Practices....................................................................................... 16
8.0 Radioactive Waste........................................................................................................... 18
8.1 Solid Radioactive Waste Management ......................................................................... 18
8.2 Liquid Scintillation Counting Vials, Glassware, and Plastic Containers...................... 19
8.3 Radioactive Sharps........................................................................................................ 19
8.4 Liquid Waste ................................................................................................................. 20
8.5 Animal Carcasses .......................................................................................................... 21
i
8.6 Unacceptable Methods of Radioactive Waste Disposal ............................................... 21
8.7 Mixed Wastes................................................................................................................ 22
Generator responsibilities ................................................................................................... 23
Appendix A: Responsibilities for Radiation Safety ........................................................... 23
Radiation and Laser Safety Committee Responsibilities .................................................... 23
Division of Research Safety and Radiation Safety Officer Responsibilities ...................... 24
Principal Investigator/Unit Head Responsibilities .............................................................. 27
Worker Responsibilities ...................................................................................................... 28
Appendix B: Recommended Procedures ............................................................................ 29
Contamination Survey Procedures...................................................................................... 29
Personnel Dosimetry ........................................................................................................... 32
Declaration of Pregnancy.................................................................................................... 33
Radioactive Waste Contents Tags Procedure ..................................................................... 33
Records required to be kept in the laboratory ..................................................................... 35
Appendix C: Fact Sheets for Commonly Used Isotopes .................................................... 38
Tritium 3H ........................................................................................................................... 39
Carbon 14C .......................................................................................................................... 40
Phosphorus 32P .................................................................................................................... 41
Phosphorus 33P .................................................................................................................... 42
Sulphur 35S .......................................................................................................................... 43
Chromium 51Cr.................................................................................................................... 44
Technetium 99mTc ............................................................................................................... 45
Iodine 125I ............................................................................................................................ 46
Iodine 131I ............................................................................................................................ 47
Appendix D: Abbreviations, Conversions, Examples and Formulas ............................... 48
Appendix E: Recommended Forms .................................................................................... 50
RADIATION PERMIT APPLICATION ........................................................................... 51
SURVEY LOG ................................................................................................................... 55
Radioisotope Use and Waste Log ....................................................................................... 56
DECLARATION OF PREGNANCY................................................................................. 57
Recommended Reading for Pregnant Female Radiation Workers ..................................... 58
Appendix F: Glossary ........................................................................................................... 67
Index ....................................................................................................................................... 76
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1.0 Introduction
The purpose of this manual is to present regulations and recommended procedures for
working with radiation sources at the University of Illinois at Urbana-Champaign to protect
the individual, prevent the spread of contamination, and assist the university in fulfilling its
responsibilities to its students, staff, and neighbors.
This manual is designed to help staff members perform teaching, research, and public service
with radiation sources in a safe, legal, and efficient manner. It is a general resource on rules,
procedures, and responsibilities for working with radiation. Because of the wide variety of
radiation sources, facilities, research methods, and situations; it is impossible to anticipate
and address all eventualities within the scope of this manual.
This manual is written primarily for personnel working with beta/gamma-emitting

radioactive material. Additional requirements may be necessary for work with radioisotopes,
which decay by alpha emission or by spontaneous fission. Materials containing natural
radioactivity in concentrations not exceeding that of natural potassium (10-9 curies/gram) are
exempt from regulatory control.
The individual radiation user is responsible for understanding and conducting operations in a
manner to minimize hazards to self and others.
The principal investigator (PI), also referred to within this manual as “laboratory supervisor”
or “permit holder,” is responsible for ensuring that all personnel in his/her area receive
instructions on the nature of the radiation hazards and the necessary radiation safety
procedures in the laboratory. Radiation workers must possess the necessary skills and
disposition to cope with radiation safety problems.
The Division of Research Safety (DRS) provides consultation and services related to
radiation safety to users and laboratory supervisors.
The Radiation and Laser Safety Committee, a standing committee of the Office of the
Chancellor, is responsible for establishing policies for the Radiation Safety Program, for
reviewing the work of DRS staff, and for advising them and the radiation users on specific
problems.
All individuals using radiation sources, and their supervisors, must familiarize themselves
with the portions of this manual that apply to their operations.
Appendix A of this manual gives a more detailed description of these responsibilities.
University of Illinois Radiation Safety Manual Revision Date: April 2014 Page 1
2.0 Authorization of Ionizing Radiation Sources
The procurement, possession, or use of radioactive material is permitted only pursuant to a
Radiation Permit issued by DRS. A permit is also required for technologically “enhancing”
naturally occurring radioactive material. This section of the manual discusses the application
process, responsibilities for maintaining a permit, steps to amend or terminate a permit, and
the policy on abandoned radioactive materials.
2.1 Radiation Permit Application Process
Appendix E of this manual has a copy of the Radiation Permit Application. Complete the
application and submit it to DRS.
DRS reviews the application, prepares a radiation permit specifying the quantities, locations
and conditions for use of radioactive materials, and obtains the approval signatures of the
campus Radiation Safety Officer and the Radiation and Laser Safety Committee Chair. The
permit is then returned to the applicant in duplicate. The PI and his or her unit head must sign
and return one copy of the permit to DRS, thereby acknowledging their acceptance of the
responsibilities associated with the permitted activities. The other copy of the permit is
retained by the PI and must be made available to persons using radiation sources under its
provisions.
Once all signatures have been obtained, the permit is in effect and procurement of radioactive
materials may commence (see section 4.0). Before operations under the permit commence,
DRS personnel will inspect the laboratory to ensure that the area is properly posted, waste
cans and radiation detectors are available, and other conditions specified in the permit are
met.
2.2 Radiation Permit Validity
A permit is valid as long as the conditions in the permit are fulfilled and there is a need for
radioactive materials in the laboratory. In some cases, a PI may need a radiation permit for a
specified period of time. At the end of that time, the permit should be deactivated in
accordance with section 2.4. If no radioactive material usage is planned for several months or
more, the PI should request that the permit be deactivated.
2.3 Amendments
A permit can be amended at any time, e.g., to include additional types or quantities of
radionuclides. To do this, the PI sends a written request describing the desired change to
DRS. DRS evaluates the change. If the amendment is approved, the Radiation Safety Officer
authorizes the new permit, and a copy is sent to the PI. Additional signatures are not
required.
Authorization of Ionizing Radiation Sources 2.0
2.4 Deactivating/Reactivating a Permit
A laboratory must be free of any radioactive material (in the form of contamination, source
vials, waste or stored samples) before a permit can be deactivated. Radioactive material must
be properly disposed or transferred to another laboratory with an authorized permit as
described in Section 4.3. Laboratory personnel should perform surveys to ensure that no
contamination exists in the lab. Once surveys have shown that the laboratory is free of
contamination, laboratory personnel should remove or deface radioactive labels and
markings. DRS personnel should then be contacted to perform a final survey and remove the
radioactive material postings from the laboratory entrances. The permit is deactivated when
all areas have received a satisfactory final survey and postings have been removed.
A PI can simply reactivate a previously deactivated permit by contacting DRS. No additional

signatures are required to reactivate a permit.
2.5 Abandoned Radioactive Materials
Campus units are responsible for decontaminating facilities and for identification and proper
disposal of radioactive materials abandoned by their personnel.
Situations may arise in which unknown or abandoned radioactive materials and/or

contamination are discovered. In such cases, the campus unit is responsible for performing
detailed analyses and disposing of such materials and/or reducing contamination to
acceptable levels as stipulated by regulatory agencies. If a campus unit is not able to assume
these responsibilities or perform these required tasks within a reasonable time frame, it may
enlist the services of a qualified outside vendor or DRS on a cost-reimbursement basis).
If unknown or abandoned radioactive material or contamination is discovered, DRS will

request the responsible campus unit in writing to effect cleanup within 60 days. After 60
days, DRS may assume responsibility and proceed to complete the task unless DRS and the
responsible campus unit agree otherwise. The campus unit will reimburse DRS for the costs
incurred in the process. The Radiation and Laser Safety Committee will arbitrate any
disputes that may arise.
Further questions concerning this policy should be directed to DRS, telephone 217-333-2755.
3.0 Radiation Safety Training Requirements
Each PI is responsible for providing radiation safety training to persons using radiation
sources under his or her supervision at intervals not to exceed 12 months. Regulations also
require each PI to provide awareness training at the same interval for anyone who frequents
radioactive materials locations that are under his or her supervision. Other individuals may
provide the training under the supervision of the PI. DRS has developed web-based training
modules that give a general background in radiation safety and can provide general training
to personnel upon request.
The law requires that individuals shall be instructed in the following topics before working
with radioactive materials:
• Health protection problems associated with exposure to radioactive materials or
radiation;
• Precautions or procedures to minimize exposure;
• Purposes and functions of protective devices employed;
• The permit conditions and the applicable portions of the Radiation Safety Manual;
• Employee responsibility to promptly report any condition that may lead to or cause
a violation of the regulations or cause an unnecessary exposure;
• Actions to take in the event of an emergency;
• Radiation exposure reports that workers may request.
Particular attention should be given to contamination survey requirements, dosimetry

requirements, necessary documentation, safety precautions/equipment, authorized
radionuclides, possession limits, precautions during pregnancy, and locations where
radioactive materials are authorized. State rules require that this knowledge be reinforced by
annual radiation safety training.
The extent of the instruction shall be commensurate with the potential radiological health
problems in the work area.
Records of this instruction must be maintained by the PI for audit by DRS personnel or for
inspection by state regulatory personnel.
4.0 Procurement and Transfer of Radioactive Materials
4.1 Ordering Radioactive Materials
Only holders of current radiation permits may order radioactive materials. The permit
specifies the conditions, limitations, isotopes and quantities, under which the approved user
may possess and use the specific radioisotopes being purchased.
To purchase radioactive materials, the PI submits a completed university purchase requisition

to his/her business office. The purchase requisition should be labeled “Radioactive
Material.” The PI’s campus unit must initiate a purchase requisition or standing purchase
order for the radioactive materials in the Banner or I-Buy System. Then the unit must enter
the applicable information into DRS radioactive material purchasing database for final
authorization. DRS database may be accessed from:
https://www.drs.illinois.edu/DrsDRS/PI/PIMain.aspx
To ensure expeditious handling of the order, the PI should provide the following information
on the university purchase requisition:
a. The name and signature of the PI responsible for the materials,
b. The isotope being ordered,
c. The amount of activity in millicurie (mCi) or microcurie (μCi) units being ordered,
d. The chemical form of the isotope being ordered.
Unless previous arrangements have been made, all radioactive materials shall be shipped to:
Division of Research Safety
Special Materials Storage Facility, MC-612
ATTN: PI/Permit Number
2006 South Griffith Drive
Champaign, Illinois 61820
4.2 Receipt of Radioactive Materials
Unless prior arrangements have been made, DRS at the Environmental Health and Safety
Building receives all campus orders of radioactive material. DRS monitors all shipments in
accordance with regulations established by the Illinois Emergency Management Agency
(IEMA). After each shipment of radioactive materials has been checked and found to be in
compliance with all applicable rules and regulations, DRS personnel deliver it to the user’s
laboratory during workdays, usually between 10 a.m. and 2 p.m.
DRS provides a Radioactive Material Receipt Record for each package delivered. The person
accepting the material is asked to sign for the package(s).
Procurement and Transfer of Radioactive Materials 4.0
Laboratory personnel should use a wipe test to check the inner container and determine
whether leaking has occurred. Shipments containing materials that may be volatile, gaseous,
or readily dispersible shall be opened in a fume hood. The user shall notify DRS immediately
if there is a problem with the shipment.
Upon receipt of a new shipment, laboratory personnel should enter pertinent data in a
Radioisotope Use and Waste Log (see Appendix E).
Laboratory personnel must dispose of the shipping material in an appropriate manner. If

contamination is present, place the material in a radioactive waste container. If the shipping
material is free of contamination, remove or deface any "radioactive materials" labels or
markings on it and dispose of it in the regular trash or recycle.
4.3 On-campus Transfers of Radioactive Materials
Transfers of radioactive materials within the campus may occur between mutually agreeable
PIs after authorization by DRS. These are regarded as “on-campus” transfers. A PI is not
permitted to dispense radioactive materials on a routine basis to other researchers. DRS will
approve procedures for recurrent transfers of radioactive materials over a period of time on a
case-by-case basis. The following describes the steps to transfer radioactive material:
GIVER:
1. Request permission by contacting DRS with the following:
a. Radiation permit number and name of the individual to receive the materials;
b. Location where materials will be used/stored by the recipient;
c. Isotopes and amounts (mCi) to be transferred.
2. Ensure that the material is properly packaged for transport.
3. Maintain written records of all transfers, including isotopes, amounts, dates, and
documentation of contamination surveys of packages.
RECEIVER:
Maintain accurate records of the receipt (isotope, quantity, date, from whom that material
was received). Ensure that the radioactive material is stored properly.
Procurement and Transfer of Radioactive Materials 4.0
4.4 Off-campus Transfers of Radioactive Materials
Transfers of radioactive material to off-campus personnel may be done only via DRS. DRS
personnel ensure that the radioactive material is properly packaged and in compliance with
shipping regulations. All such shipments are handled on a case-by-case basis. Contact DRS
personnel at 217-333-2755 for assistance.
4.5 Transfers of Radioactive Materials from Off-campus
Occasionally, a PI may receive radioactive material as a gift from another campus or

institution where a purchase order is not involved. In such cases, the PI must make prior
arrangements with DRS for purposes of license verification, radiation permit authorization,
and receipt instructions.
5.0 Using Radioactive Materials
5.1 Storage of Radioactive Materials
Radioactive materials must be secured at all times. This may be accomplished by any of the
following:
1. Attending the materials,
2. Maintaining materials in a locked freezer or cabinet,
3. Locking the room in which the materials are stored.
These requirements apply to all radioactive materials in the laboratory, including waste,
contaminated equipment, and sealed sources.
Radioactive materials stored in occupied areas shall be shielded in accordance with the
ALARA principle (i.e., radiation exposures to faculty, staff, students and the public resulting
from the use of radiation sources in teaching and research shall be kept As Low As
Reasonably Achievable (ALARA)), which is discussed in Sections 7.8 and 7.9.
Unbreakable containers are recommended for storing radioactive liquids. Glass or fragile
bottles and other breakable containers used for storage must be kept in non-breakable, leak-
proof secondary containers or trays capable of containing the entire volume of liquid stored
in the primary container.
Radioactive gases and volatile forms of radioisotopes should be stored in a well-ventilated

area, such as a fume hood.
Sealed sources must remain in the same condition as received from the manufacturer. No
modification of sealed sources is permitted without express written consent from DRS.
Sealed sources that have been mutilated and damaged beyond what would reasonably be
expected to occur as a result of its normal use should be reported to DRS as soon as possible.
Radioisotopes and calibration sources shall be clearly labeled with the following information:
Caution: Radioactive Materials

Radionuclide
Activity and assay date
Person responsible for sample or source
Labeling is not required if the activity is less than the following:
Using Radioactive Materials 5.0
Nuclide Quantity (μCi)

H-3 1000
C-14 1000
P-32 10
P-33 100
S-35 100
Tc-99m 1000
I-125 1
I-131 1
Exemptions for other radionuclides may be found in Appendix C of the Code of Federal
Regulations, Title 10, Part 20.
http://www.nrc.gov/reading-rm/doc-collections/cfr/part020/part020-appc.html
5.2 Using Radioisotopes in Animals
When radioisotopes are used in animals, the areas in which animals are kept must be posted
in accordance with the requirements of IEMA statutes and regulations.
Cages and pens must bear labels listing the isotope used, the quantity and date administered,
measured external radiation levels, and the name of the PI. These cages and pens should be
separated from those housing non-radioactive animals.
Ventilation should be adequate to handle the possibility of airborne radioactivity. In some

instances, this may require the use of a fume hood or self-contained, controlled
environmental systems.
Procedures for disposal of animal excreta must be included in the radiation permit
application process. If excreta are mixed with bedding materials, handle in accordance with
dry radioactive waste procedures.
DRS must approve disposal methods for animal carcasses.
Animal caretakers shall be instructed and trained by the PI on handling procedures, dose
levels, occupancy time limits, and applicable special conditions. Animal caretaking should
be performed by trained research personnel.
Authorization to administer radioisotopes to animals shall be approved by DRS. DRS

establishes the criteria for releasing the animals to the owners.
6.0 Emergency Procedures
In any radiation emergency, personnel protection comes first, confinement of radioactivity

next.
In an emergency, immediately notify DRS at 3-2755 from university telephones or 217-333-

2755 from personal telephones)) because the emergency may demand immediate action by
those on the scene. Refer to the guidelines in this section.
These guidelines are intended to help users to develop a safety-oriented attitude, actively
anticipate and work to prevent potential hazards and accidents and to respond appropriately
to unexpected events. The PI may find it useful to draw up a written emergency plan suited to
his/her own facility and operations. The PI should make the specific equipment and supplies
required to minimize hazards and enhance recovery readily available. For example, chemical
compounds in use might require special decontamination agents.
6.1 Serious Injury and Exposure or Contamination
If someone has received high radiation exposure or radioactive contamination in addition to

physical injury requiring immediate medical assistance, call MetCAD (911 from any
university or personal telephone). Inform emergency personnel that the patient is/might be
contaminated.
If possible, someone familiar with the incident should accompany the injured person to
provide information such as the nature of the injuries, radiation levels, and the physical and
chemical nature of the contamination. Also, follow instructions listed in 6.4 for Intermediate
and High-Level Spills.
6.2 Fire or Explosion in a Radioisotope Area
In case of fire or explosion, call MetCAD (911 from any university or personal telephone). If
possible, stay on the scene at a safe distance to provide the fire officer in charge with
information on the nature of the radiation hazards present and to assist him/her as required.
Also, follow instructions listed in 6.4 for Intermediate and High-Level Spills.
Emergency Procedures 6.0
6.3 High Radiation Exposure Without Contamination
Do what can be done to terminate or limit the exposure and to prevent others from being
exposed. If there is a significant exposure to all or any part of the body, notify the campus
radiation safety officer (3-2755 from university telephones or 217-333-2755 from personal
telephones).
6.4 Intermediate and High-Level Radioactive Spills
In case of a serious accident involving contamination of personnel or equipment (including

6.1 and 6.2), the following steps should be taken in the order listed.
1. Protect Personnel
a. If the hazard is extreme (high radiation level or possibility of air contamination),
evacuate the area immediately and close and lock the door.
b. Rid the victim of contamination: Remove contaminated clothing and wash
contaminated parts of the body thoroughly with mild detergent. Bag contaminated
items.
c. Flush out any wounds with copious amounts of water.
d. Warn fellow workers and keep others out of the area.
2. Confine Contamination
a. Localize the spill area. Turn containers upright that have tipped over and place
absorbent material at edges of liquid spills.
b. Do not spend time in the area of a dry spill without respiratory protection. Shut off or
close the ventilating system if possible and turn off fans and blowers on hoods.
c. Minimize the spread of contamination. Remove shoes or put on shoe covers at the
edge of contaminated area when summoning help.
d. If contamination is widespread outside the laboratory, it may be necessary to call the
University Police (telephone 3-8911 from university telephones or 217-333-8911
from personal telephones) to assist in establishing traffic control.
e. Check all objects and clothing for contamination before leaving the area. This
includes clothing, tools, equipment, or other personal effects not worn during the
accident.
f. Call DRS (telephone 3-2755 from university telephones or 217-333-2755 from
personal telephones) as soon as possible.
g. In all cases, consult the Emergency Call List posted in or near every radiation
laboratory.
3. Decontaminate
a. Abortive attempts at decontamination can make things much worse. Unless
immediate action is required to safeguard personnel and equipment, decontamination
should be done under the supervision of DRS.
Emergency Procedures 6.0
b. DRS will determine the procedures and equipment to be used and provide assistance
as necessary.
c. All personnel and areas involved must be monitored to assure adequate
decontamination before normal work is resumed.
After the emergency has passed, the individuals involved shall cooperate fully with DRS
personnel in an incident investigation.
Personnel Exposure 7.0
7.0 Personnel Exposure
7.1 Occupational Exposure Limits
1. The annual limit for occupational workers is the more limiting of:
a. The total effective dose equivalent = 5,000 millirem (0.05 Sv); or

b. The sum of the deep dose equivalent and the committed dose equivalent to any
individual organ or tissue (other than the lens of the eye) = 50,000 millirem (0.5 Sv).
2. The annual limits to the lens of the eye, to the skin, and to the extremities are:
a. Eye dose equivalent = 15,000 millirem (0.15 Sv)

b. A shallow dose equivalent = 50,000 millirem (0.5 Sv)
7.2 Non-Occupational Exposure Limits (Members of the Public)
Each user of radioactive material shall conduct operations so that:
1. The dose in any unrestricted area from external sources does not exceed 2 millirem (0.02
mSv) in a hour.
2. The total effective dose equivalent to individual members of the public from a licensed
operation, exclusive of the dose contribution from a licensee’s disposal of radioactive
material into sanitary sewerage, does not exceed 100 millirem (1 mSv) in any year.
7.3 Declared Pregnant Workers Exposure Limits
The dose limit to an embryo/fetus during the entire pregnancy due to occupational exposure
of a declared pregnant woman is 500 millirem (5 mSv). Care shall be taken so that no more
than 50 millirem (0.5 mSv) be received during any one month during a declared pregnancy.
Efforts shall be made to avoid substantial variation above uniform monthly exposure rate to a
declared pregnant woman (see Appendix B for additional information).
If the pregnant woman has not notified DRS of her estimated date of conception, the dose to
the fetus shall not exceed 50 millirem (0.5 mSv) per month during the remainder of the
pregnancy.
If, by the time the woman informs DRS of the estimated date of conception, the dose to the
embryo/fetus has exceeded 450 millirem (4.5 mSv), the limit for the remainder of the
pregnancy shall be 50 millirem (0.5 mSv).
7.4 Exposure Limits for Minors
The annual occupational dose limits for minors are 10 percent of the annual occupational
limits specified for adult workers in Section 7.1 of this manual.
7.5 When Dosimetry Is Required
The IEMA requires dosimetry for the following:
1. Adults likely to receive in one year a dose in excess of 10 percent of the occupational
exposure limits from sources external to the body (Section 7.1).
2. Minors and declared pregnant women likely to receive in one year a dose in excess of
10 percent of the applicable limits from sources external to the body (Section 7.3 or
Section 7.4).
3. Individuals entering a high or very high radiation area.
DRS assigns dosimetry when certain quantities and nuclides are used. Specifically, the use of
>10 mCi of P-32 requires the user to wear both an extremity (commonly referred to as a
“ring”) and a whole-body dosimeter. At usage levels ≤10 mCi of P-32, dose assessments will
be performed to evaluate the need for dosimetry.
DRS evaluates the use of dosimetry with other radionuclides and quantities on a case-by-case
basis.
7.6 Bioassays
Bioassays, analyses, or evaluations of materials excreted or removed from the body are
required to determine types, concentrations, quantities, or locations of personal uptake. A
baseline (before first use) bioassay and another within 24 to72 hours following each use of
the quantities specified is required. Thyroid bioassays are performed using a hand-held
scintillation probe and survey meter. Tritium bioassays are performed by condensing water
from exhaled air. DRS personnel perform bioassays at the following location if other
arrangements are not made:
Environmental Health and Safety Building

101 South Gregory Street, Urbana
Users of unbound radioactive iodine (typically I-125 or I-131) in quantities of ≥1 mCi on a

bench top or in quantities ≥10 mCi in a fume hood require thyroid bioassays. These bioassays
are performed on a walk-in basis during business hours unless previous arrangements are
made. Tritium bioassays are required when a person uses >100 mCi of H-3 without using a
fume hood. DRS must be notified at least 24 hours in advance for this and the baseline
tritium bioassay.
Additional bioassays may be required for personnel on a case-by-case basis as determined by

DRS.
7.7 Personnel Exposure Records
DRS maintains exposure records for all monitored personnel. Annual reports of exposure are
sent to personnel required to wear dosimetry in accordance with Section 7.5.
At the request of a worker, DRS shall furnish his or her exposure report. The report is
furnished within 30 days from the time the request is made, within 30 days of termination of
employment, or within 30 days after the individual’s dose has been determined, whichever is
later.
7.8 ALARA (As Low As Reasonably Achievable)
The university is committed to maintaining radiation exposures to faculty, staff, students, and
the public resulting from the use of radiation sources in teaching and research As Low As
Reasonably Achievable (ALARA). The Radiation and Laser Safety Committee and DRS
advise and assist faculty, staff, and students in all matters regarding radiation safety. The
committee recommends to the campus administration, through DRS, policies and procedures
for maintaining ALARA radiation exposures through the safe handling, storage, use,
transport and disposal of radiation sources. It will assist in the interpretation of the rules and
regulations of the U.S. Nuclear Regulatory Commission, the IEMA, the U.S. Environmental
Protection Agency, the U.S. Center for Devices and Radiological Health, and others that
pertain to protection against radiation.
Sources of radiation include materials or equipment that are capable of emitting either
ionizing or non-ionizing radiation. Ionizing radiation sources include radioactive materials,
nuclear reactors, particle accelerators, X-ray machines, and electron microscopes. Non-
ionizing radiation sources include lasers, high-intensity sources of ultraviolet light,
microwave transmitters and other devices that produce high intensity radio-frequency
radiation. Both types of radiation are of concern and are under the purview of the Radiation
and Laser Safety Committee and DRS.
7.9 Exposure Reduction Practices
Use the concepts of time, distance, and shielding to minimize personnel exposure.
To prevent accidental entry of radioactive materials into the body, high standards of
cleanliness and good housekeeping must be maintained in all laboratories where radioactive
material is present. Wash hands and arms thoroughly before handling any object that goes
into the mouth, nose or eyes (e.g., cosmetics, foods, contact lenses). Keep fingernails short
and clean. Never pipette by mouth; instead use rubber bulbs, syringes or mechanical devices.
Clean up minor spills immediately. For major spills, follow emergency procedures.
Visitors are not allowed into the lab without approval of the PI.
Smoking, eating, drinking, and applying cosmetics in radioisotope laboratories are not
allowed. Refrigerators shall not be used jointly for foods and radioactive materials.
For new procedures and new personnel, one or more trial runs beforehand with non-
radioactive materials are recommended to test the effectiveness of procedures, training, and
equipment.
Use appropriate shielding. Do not use lead shielding for beta-emitting nuclides.
Always use gloves when handling unsealed radioactive materials. Wear protective clothing
(lab coats, eye protection, shoe covers) as needed. Do not work with unsealed radioactive
materials if there is a break in the skin below the wrist.
Tritium users: Change gloves every hour when working with 50 mCi or more.
Whenever possible, operations with radioactive materials should be conducted in a hood, dry
box, or some other type of closed system. Operations with materials susceptible to
atmospheric distribution, such as boiling, evaporating, distilling, or ashing, must be done in a
fume hood with airflow of approximately 100 linear feet per minute. Fume hoods in
radioactive material laboratories are checked periodically for airflow and the proper sash
height is indicated on the fume hood. Work with nuclides with half-lives of more than a few
hours should be done over a containment to prevent the spread of contamination in the event
of a spill. Work with radioactive materials in powder form should be done in an enclosed
system.
Table and bench tops should be of a non-porous, chemical-resistant material. Working

surfaces should be covered with absorbent paper regardless of the type of surface.
When work is completed, each user should clean up his/her own work area and arrange for
disposition of all radioactive materials and equipment.
Vacuum pumps used in systems containing radioisotopes should be used in fume hoods with
proper flow rates.
External exhaust stacks must not be vented towards windows or building air intake vents.
Laboratories shall provide non-leaking radioactive waste containers bearing the words
"Caution: Radioactive Materials."
University cleaning crews are permitted to clean floors and windows only. Laboratory
personnel are responsible for the remainder of the housekeeping.
Repairs on potentially radioactive systems such as sink drains and fume hoods should not be
undertaken unless DRS personnel have released the area or item from radiological control.
8.0 Radioactive Waste
8.1 Solid Radioactive Waste Management
Solid radioactive waste is disposed of by land burial at licensed, low-level radioactive waste
facilities or by holding short-lived wastes for radioactive decay until their radiation levels are
indistinguishable from background, and then disposing of them as ordinary waste. Because
the availability of land burial sites is subject to political and technical limitations, and the
space available for decaying short-lived wastes is limited, radioisotope users should make
every effort to minimize the volume of radioactive wastes generated in their laboratories.
All solid radioactive waste is packaged by users and then transferred to DRS personnel for
treatment by decay-in-storage or other method of final disposal.
As much as possible, wastes shall be segregated according to isotopes. It is especially

important to segregate dry wastes containing tritium (H-3) and carbon-14 (C-14) from other
long-lived isotopes.
Solid wastes should be collected, stored, and packaged in containers lined with plastic bags
with a thickness of at least four mils of LDPE, clear or transparent yellow in color, and
bearing the radiation hazard symbol. The containers shall be labeled with the radiation hazard
symbol and the words “Caution–Radioactive Material”. Individual bags should be no greater
than 30 gallons in volume. Laboratories are responsible for providing their own disposal
containers and bags.
No freestanding liquids, lead, sharps or animal carcasses/tissue may be disposed of in solid

wastes. If lead cannot be decontaminated, it should be packaged separately for collection. See
section 8.3 for handling of radioactive sharps.
Activities that generate wastes that are classified as both hazardous chemical wastes and
radioactive wastes may not be initiated without specific approval from the Radiation and
Laser Safety Committee or DRS.
It is the responsibility of the laboratory personnel to comply with the segregation, collection,
packaging, and labeling requirements and to secure all wastes for removal from the
laboratory. DRS may refuse any package that does not conform to the requirements of this
section or which, in their opinion, may present a safety hazard to waste-handling personnel or
members of the public.
Radioactive Waste 8.0
Prior to pick-up by DRS, each container must have a completed Radioactive Waste tag
attached to it. These tags are available from DRS. Appendix B gives instructions for
completing these tags. When waste has been properly prepared, log on to DRS website at:
http://www.drs.illinois.edu/radiationsafetyapp/Waste/PickupRequest.aspx/ and complete the
online pickup request.
8.2 Liquid Scintillation Counting Vials, Glassware, and Plastic Containers
Empty liquid scintillation counting vials that contained media in which the concentration of
C-14 or H-3 is less than 0.05 microCurie per milliliter (μCi/ml) need not be decontaminated
and should be disposed of with the regular, non-radioactive solid waste. Ensure that vials have
been properly emptied and “radioactive material” labels have been removed or defaced.
Empty vials containing radioactive materials other than C-14 or H-3 must be held for decay
or decontaminated.
After contaminated vials have been washed, a representative sample of the wash water
should be counted to determine the effectiveness of the washing. If the average count rate is
less than twice the background level, dispose of the containers in the non-radioactive waste.
Containers that cannot be sufficiently decontaminated must be disposed of in the solid
radioactive waste after having been properly emptied and dried. Wash water may be disposed
if conditions in Section 8.4 are met.
Most glass items (e.g., test tubes, dishes) can be decontaminated by routine washing or an
overnight soaking with an industrial-strength detergent and re-used.
8.3 Radioactive Sharps
Radioactive sharps are hazardous items that require special precautions and handling. If the
following items have come into contact with radioisotopes, dispose of them in containers
specifically designed for sharps that bear a Caution–Radioactive Material label listing
isotope and date:
• Needles and syringes,
• Pasteur pipettes,
• Scalpels and razor blades,
• Microscope slides and coverslips,
• Glassware that cannot be decontaminated.
Sharps containers are closable, puncture-resistant, leak-proof on the sides and bottoms, and
are typically available in 1-quart, 2-gallon, and 8-gallon sizes.
Most glassware, such as liquid scintillation vials and test tubes, is easily decontaminated as
described in section 8.2 and should not be routinely discarded as sharps.
When sharps containers are full and properly tagged, enter the appropriate information for
pickup and disposal on DRS website at http://www.drs.illinois.edu/regwaste/rad/index.aspx.
8.4 Liquid Waste
There are two main types of liquid radioactive wastes generated by research laboratories. The
most common liquid waste is aqueous, in which the waste materials are dissolved in water.
Such waste may be disposed of by dispersal into the sewage system if concentration limits
are low enough. Designate and label a sink for this purpose. The pH range of any aqueous
waste shall be adjusted to between 6.8 and 8.0. Aqueous wastes shall not exceed the
following concentrations:
Radionuclide Concentration (μCi/ml)

H-3 1 x 10-2
C-14 3 x 10-4
P-32 9 x 10-5
P-33 8 x 10-4
S-35 1 x 10-3
I-125 2 x 10-5
I-131 1 x 10-5
Other radionuclide concentration limits can be found in Title 10, Code of Federal
Regulations, Part 20, Appendix B, Table 3.
The other, less common form of liquid radioactive waste is composed of volatile, flammable,
toxic or organic material that cannot be disposed of through the sewage system. Water
insoluble organic solvents shall not be released into the sewage system under any
circumstances. (Toluene and xylene-based liquid scintillation cocktails and some HPLC
fluids fall into this category. Users are advised to use water-soluble fluids whenever
possible). Non-aqueous waste shall be free of all filterable solids. For filtering liquid
scintillation waste, a 60-mesh metal screen is recommended. Organic, water-insoluble liquid
waste is then collected by DRS personnel for disposal. Non-aqueous waste shall be stored in
spill-proof, unbreakable plastic containers of either six or ten liter capacities.
Liquid wastes that do not fit into the above categories must be treated on a case-by-case
basis. See also Section 8.7 Mixed Wastes
CAUTION:
Problems involving chemical reactions between mixtures of liquid wastes may occur.
Disposing of cyanides in acidic liquid waste will produce hydrogen cyanide, a very toxic
gas. Special care must be taken when disposing of tissue that has been digested in nitric
acid, as oxides of nitrogen may be formed that could cause the waste container to explode.
The PI must ensure that chemical reactions will not occur in liquid waste containers.
DRS personnel reserves the right to refuse to accept any materials if, in its opinion, the
materials have been improperly prepared or packaged or if they think that the movement of
the materials would pose an unacceptable hazard to workers, other members of the campus
community, or the public.
Each container of liquid waste should have a waste tag attached to it. Procedures for
completing waste tags can be found in Appendix B.
8.5 Animal Carcasses
Radioactive material used in animals must be handled on a case-by-case basis. PIs planning
to administer radioactive material to animals should contact DRS for guidance concerning
the disposal of carcasses.
Animal tissues containing 0.05 µCi or less of hydrogen-3, carbon-14, or iodine-125 per gram
of animal tissue averaged over the weight of the entire animal can be disposed of as if it were
not radioactive. However, animal tissue in which radioactive materials have been introduced
shall not be disposed in a manner that would permit its use either as food for humans or as
animal feed, such as rendering.
8.6 Unacceptable Methods of Radioactive Waste Disposal
No freestanding liquids, lead, sharps, or animal carcasses/tissue may be disposed of in solid

wastes.
Under no circumstances shall personnel bury radioactive waste in the soil.
Under no circumstances shall non-aqueous radioactive waste be released into the sewage
system.
Aqueous radioactive liquids in excess of the concentrations specified in Section 8.4 shall not
be released into the sewage system. The liquid must either be held for decay or turned into
dry waste and packaged appropriately.
Carcasses or animal tissues in which radioactive materials have been introduced shall not be
disposed of by rendering (a manner that would permit its use either as food for humans or as
animal feed).
8.7 Mixed Wastes
Mixed wastes are defined as wastes that contain radioactive materials and a hazardous waste.
These types of wastes require special handling. Researchers are encouraged to minimize the
generation of mixed wastes because of the high disposal costs.
Radioactive wastes that contain any of the following must be handled as a mixed waste:
Solvents (e.g., methanol, methylene Carbon Tetrachloride

chloride, acetone) Chlordane
Flammable chemicals Chlorobenzene
Nitrates Chloroform
Sulfides O-Cresol
Cyanides M-Cresol
Aqueous solutions with pH < 2 or > 12.5* P-Cresol
Arsenic 1,4-Dichlorobenzene
Barium 1,1,-Dichloroethylene
Cadmium 2,4-Dinitrotoluene
Chromium Heptachlor
Lead Hexachlorobenzene
Mercury Hexachlorobutadiene
Selenium Hexachloroethane
Silver Methyl Ethyl Ketone
Endrin Nitrobenzene
Lindane PCBs
Methoxychlor Pentachlorophenol
Toxaphene Pyridine
2,4-D Tetrachloroethylene
2,4,5 TP (Silvex) Trichloroethylene
Benzene 2,4,5-Trichlorophenol
*If pH is the only item on this list that 2,4,6-Trichlorophenol
makes the item a mixed waste, it can be Vinyl Chloride
neutralized and handled as Rad Waste.
If the waste contains I-125, P-32, or S-35 isotopes in addition to anything listed above, the
waste should be retained by the generator until it is adequately decayed (typically 10 half-
lives) so that it no longer qualifies as a regulated radioactive waste. Then the waste can be
classified as chemical waste only. The appropriate CWM-TRK form should be used by the
generator to request a pickup.
If the waste contains C-14 or H-3 isotopes in addition to anything listed above, the following
procedures should be followed:
Generator responsibilities
1. The generator submits a CWM-TRK form to request a pickup. If unsure which form
to complete or which UI# to use, contact DRS personnel for assistance. Forms are
available at: http://www.drs.illinois.edu/css/guidesplans/wasteguide/cwmtrk.aspx
2. A copy from the liquid scintillation printout for the particular waste should be
submitted with the CWM-TRK form. A calculation of the isotopic concentration (in
μCi/ml) and total activity (μCi) for the waste is required. If there are multiple wastes,
a copy of the printout with calculations should be submitted for each waste.
DRS personnel are responsible for the pickup and disposal of mixed wastes from campus
laboratories.
Appendix A: Responsibilities for Radiation Safety
The U of I strives to maintain a safe and healthy working and learning environment for
faculty, staff, students, and visitors. The cooperation of the entire campus community is
needed to realize this goal. This is particularly true of research and teaching that involves
radiation sources, where the Campus Radiation and Laser Safety Committee, and radiation
safety officer (RSO), principal investigators (PIs) and department heads, and laboratory
workers share the responsibility for creating and maintaining a safe workplace.
Radiation and Laser Safety Committee Responsibilities
The Radiation and Laser Safety Committee advises the Chancellor through the Vice
Chancellor for Research and the Division of Research Safety (DRS) on matters related to the
campus Radiation Safety Program. The Committee is composed of academic staff and
faculty members representing various areas of research and teaching, and members who
represent the campus administration including the campus RSO.
The chancellor delegates authority to the committee to oversee the use of radiation sources
throughout the campus. The committee has the authority to permit, deny, or revoke
authorization for individuals to obtain and use radiation sources at the U of I.
The responsibilities of the Radiation and Laser Safety Committee include the following:
1. Review proposals for unusually hazardous uses of radiation sources as deemed by the
RSO, and establish criteria for equipment and procedures to ensure employee,
student, and public safety.
2. Review cases that involve repeated infractions of the rules and regulations for
protection against radiation, including lasers.
3. Review accidents that may involve exposure or serious economic loss and other cases
for which reports to outside regulatory authorities are required.
4. Review public relation problems that involve radiation sources and lasers.
5. Review appeals from radiation users and modify rules or the decisions of DRS
personnel where necessary.
6. Meet formally as often as necessary, but at least four times per year, to review the
campus radiation safety program with DRS personnel.
7. Recommend the establishment or modification of campus radiation and laser safety

policies.
8. Work with DRS to effectively use electronic communication to keep committee

members abreast of unusual events between committee meetings.
9. Review communications between DRS and government agencies that affect the
campus radiation safety program and the campus radioactive materials license.
Division of Research Safety and Radiation Safety Officer Responsibilities
1. Provide advice and assistance to all concerned on all aspects of radiation safety.
2. Approve proposals for procurement, use and transfer of radiation sources except proposals
involving unfamiliar or extreme hazards that DRS judges as requiring review by the
Committee.
3. Receive and monitor all shipments of radioactive materials, deliver acceptable incoming
shipments to the consignee, and ensure that outgoing shipments conform to shipping
regulations.
4. Maintain permanent records of receipt, use, transfer, and disposal of radioactive materials.
5. Supervise and assist in disposal of radioactive wastes.
6. Assign personnel monitoring devices (e.g., film badges, dosimeters) when necessary, give
instructions in their use, and maintain personnel monitoring records.
7. Check radiation monitoring and survey instruments for proper operation and calibrate as
often as necessary.
8. Assist in designing and selecting equipment, shielding, and facilities and in the formulating
operating procedures for new or modifying existing installations or buildings.
9. Calculate the levels of radiation intensity, time limits of personnel exposure, and minimum
working distance around accelerators, reactors, X-ray machines, and other intense radiation
sources.
10. Perform and keep records of leak tests on sealed sources.
11. Make and keep records of systematic surveys in areas where the presence of radiation or
contamination of surfaces, air, or water is suspected, and notify the area supervisor of the
results. In some cases this may require detailed monitoring of an operation from beginning
to end by a DRS member.
12. Report hazardous radiological conditions promptly to the individual responsible and, when
necessary, to the immediate supervisor and the Radiation and Laser Safety Committee.
13. Supervise and assist in decontamination of all but minor spills.
14. Schedule routine medical examinations in accordance with established policy; help
establish criteria, and make arrangements for such examinations as may be required in
emergency situations.
15. Enforce all written directives of the committee.
16. Stop any operation or deny access of any individual to radiation sources in the interest of
safety. Such action must be reported verbally and in writing to the committee as soon as
possible.
17. Grant exemptions to the rules (or impose more stringent restrictions) in emergency
situations when, in the judgment of DRS, such action is necessary to reduce risk of serious
injury or economic loss. Such actions must be reported verbally and in writing to the
committee as soon as possible.
18. Maintain files of federal, state, and local licenses and registrations concerned with
radiation sources and initiate applications for renewals and/or amendments of same.
19. Determine whether a radiation incident requires a report to any governing body and
prepare such reports for the approval of the committee. Exception: If an immediate report
is required, the campus radiation safety officer shall (with knowledge and approval of the
chairman if possible) file such report with the appropriate authorities and shall provide
copies to the committee.
20. Be familiar with the federal, state, and local laws relating to radiation and be aware of
changes in such laws as they occur. Inform the committee when such changes make
modifications of policy desirable and institute necessary changes in the radiation safety
program.
Responsibilities for Radiation Safety Appendix A
Principal Investigator/Unit Head Responsibilities
In addition to assuming all the responsibilities of an individual radiation user, the PI shall:
1. Be responsible for ensuring that all personnel, particularly new personnel, who have
access to radiation sources under his/her jurisdiction, are properly instructed and that they
possess the necessary skills and disposition to cope with radiation safely. The minimum
training requirements are outlined in section 3.0.
2. Determine the types of radiation sources, equipment, facilities, and procedures needed for
his/her work.
3. Comply with all radiation permit requirements.
4. Ensure that the procedures for purchase, acquisition, use, and transfer of radioactive
materials are followed in work under his/her supervision. This includes keeping accurate
inventory and disposal records.
5. Routinely check protective equipment and instruments to ensure they are working
properly and adequately performing their intended functions.
6. Work with DRS to solve radiation safety problems unique to his/her situation and to
correct violations of federal, state or local rules and regulations.
7. Assist DRS in complying with existing laws and license requirements (maintenance of
records, preparation of reports) by providing necessary information and assistance.
8. Obtain the prior approval of the campus radiation safety officer before individuals age 18
and under are allowed to work in a radiation laboratory.
9. When away from campus for an extended period, ensure that radioactive materials and
work involving radiation sources receive adequate supervision. A PI that will be absent
from his or her laboratory for a period of three months or more must designate a
temporary supervisor and inform DRS in writing of this designation. The education,
training, and administrative authority of the person designated as temporary supervisor
must be sufficient to ensure that all safety requirements will be met and must be
acceptable to DRS.
10. Inform DRS of an intention to cease using radioactive material, an extended departure
from campus is planned, or if there is any reason the obligations in this manual cannot be
met.
11. Report lost, stolen, or missing sources of radiation to DRS. DRS is required to notify
state regulators within 24 hours after when the absence becomes known.
Responsibilities for Radiation Safety Appendix A
Unit heads shall inform DRS whenever any radiation permit holder of their unit will be
absent from campus for more than three months and whenever there are circumstances that
might require additional assistance from DRS (e.g., temporary disability).
Worker Responsibilities
The individual user has the final responsibility for the safe use of the radiation sources to
which he or she has access. He/she shall:
1. Keep his/her exposure as low as practical;
2. Wear assigned personnel monitoring devices in an approved manner;
3. Be familiar with and comply with all sections of this manual applying to his/her work;
4. Be familiar with the nature of his/her area's radiation sources, the extent of their potential
risk, and use the proper means of coping with them safely;
5. Monitor his/her area frequently for contamination.
6. Clean up minor spills immediately.
7. Dispose of radioactive waste in an approved manner.
8. See that sources, containers, and the area are properly labeled and posted.
9. Assist in maintaining required records and inventories.
10. Prevent unauthorized persons from having access to radiation sources in his/her area.
11. Protect service personnel, allowing no maintenance or repairs of area facilities or

equipment unless approved by the area supervisor and/or DRS.
12. Notify his/her supervisor and DRS of unexpected difficulties.
13. Be prepared to handle accidents or injuries with common sense.
14. Notify and seek the assistance of his/her PI and DRS as soon as possible in emergencies.
15. Take no action that would interfere with the responsibilities of his/her laboratory
supervisor.
16. Notify his/her supervisor immediately of any last, stolen, or missing source of radiation.
Recommended Procedures Appendix B
Appendix B: Recommended Procedures
Appendix B provides recommended procedures for tasks frequently performed in the

laboratory. These procedures outline acceptable methods for meeting radiation safety
requirements. The procedures are generic in nature, allowing for the diversity of research
facilities, on campus.
Contamination Survey Procedures
Surveys are performed to monitor for the presence of contamination. Minimum survey
frequencies are specified on the radiation permit. The surveys should be sufficiently
extensive to allow confidence that there is no contamination. Common places to check for
contamination are: bench tops, tools and equipment, floors, telephones, floors, door handles
and drawer pulls, and computer keyboards.
Types of Contamination
Removable contamination can be readily transferred from one surface to another.

Removable contamination may present an internal and external hazard because it can be
picked up on the skin and ingested. Fixed contamination cannot be readily removed and
generally does not present a significant hazard unless the material comes loose or is present
large enough amounts to be an external hazard.
Types of Surveys
There are two types of survey methods used: 1) a direct (or meter) survey, and 2) a wipe (or
smear) survey.
Direct surveys, using a Geiger-Mueller (GM) detector or scintillation probe, can identify
gross contamination (total contamination consisting of both fixed and removable
contamination) but will detect only certain isotopes.
Wipe surveys, using “wipes” such as cotton swabs or filter papers counted on a liquid
scintillation counter or gamma counter can identify removable contamination only but will
detect most isotopes used at the U of I. Wipe surveys are the most versatile and sensitive
method of detecting low-level removable contamination in the laboratory.
Survey Instrumentation
The portable Geiger-Mueller (GM) survey meter is best used for P-32, a high-energy beta
emitter, and other high-energy beta and gamma emitters, such as Co-60, Zn-65, Cs-137, and
U-238. A GM meter can also be used to identify areas heavily contaminated with lower
energy beta emitters, such as C-14 or S-35, for which the GM meter has a relatively low
efficiency. GM meters should not be used to survey for I-125 contamination because they
detect I-125 only when there are very high levels of contamination.
The portable thin crystal NaI scintillation survey meter should be used to locate I-125
contamination and to conduct surveys around low-energy X-ray sources such as X-ray
diffractometers and electron microscopes.
The liquid scintillation counter, used for counting wipe tests, is the most versatile counting
instrument because it has a high counting efficiency for a wide range of radionuclides. Most
LSCs provide a printout of sample results that may be used as survey record.
Gamma counters are not portable and are used to count swipes of photon emitters such as
Cr-51 or I-125.
How to Perform a Meter Survey
Prior to performing any survey, clean gloves should be worn. This prevents the possibility of
personal contamination or cross-contamination.
Perform an instrument check. To check the operation of a survey instrument, do the

following:
1. Calibration check:
Check the calibration label on the instrument and ensure the instrument is within the
calibration period. If the calibration due date has passed, contact DRS to have the
instrument re-calibrated and find another instrument to use.
.
2. Battery check:
Turn the switch on the survey meter to "BATTERY," or flip the battery switch to "ON."
The needle on the meter face should move to a position within or beyond the indicated
area on the meter face scale. Replace batteries if needed before using the survey meter.
3. Speaker check:
If there is an audio switch on the survey meter, turn it to "ON." Set the survey meter to a
scale of "X1." The survey meter should chirp or click. If the speaker does not function,
the survey meter can be used, but the surveyor will need to check the reading on the
survey meter face frequently.
4. Background check:
Go to an area with an expected low background rate. Note the count rate when the survey
meter is switched to the "X1" scale. The background rate for a GM meter should be less
than 100 counts per minute; the background reading for a NaI meter should be less than
400 counts per minute. If background readings exceed these levels, investigate the area
for unknown sources of radiation or detector contamination. Do not use the survey meter
if it does not register a background rate.
5. Instrument response check:

Hold the supplied check source (often a thorium lantern mantle) up to the probe window.
Note the counting rate. The survey meter should respond to the check source, thus
providing positive indication that the instrument is functioning properly.
Do not cover the probe surface with parafilm or other protective coating. Parafilm and
similar materials will shield the low energy betas from C-14, P-33, and S-35 and may prevent
the meter from detecting contamination.
Hold the probe window approximately 1 cm from the surface to be surveyed and move the
probe over the surface at about 1 cm/second.
Check the most common sites for contamination, such as survey meter handle, soap/towel
dispensers, drawer handles, refrigerator/freezer handles, chair edges, writing utensils, survey
record books, floors, radio dials, telephone receiver/keypad, microwave oven touch
pads/handles, doorknobs, light switches, and non-radioactive trash containers.
Record survey results in a survey log (see Appendix E). If survey results are equivalent to the
background, log the result as ‘≤ BKG’. Generally, a surface is considered contaminated if the
result is greater than the background count rate. If contamination is found, record the result
and indicate the action taken.
How to Perform a Wipe Survey
Prior to performing any survey, clean gloves should be worn. This reduces the likelihood of
personal contamination or cross-contamination.
Removable contamination is best identified by a wipe survey, which is performed by rubbing

a filter paper (approximately 45 mm in diameter) or cotton swab over the survey area with
moderate pressure. The paper or swab may be wetted with ethanol or water to increase the
collection efficiency. Usually an area of 100 square centimeters (4 square inches) is
surveyed. To monitor a larger area, take additional swipes.
If surveying for low-energy beta emitting isotopes such as H-3, C-14, P-33, and S-35.,
analyze the wipe using liquid scintillation counting.
If surveying for high-energy beta emitters (e.g., P-32), wipe samples may be counted using
either liquid scintillation counting or a GM meter.
If monitoring for low-energy gamma emitters (e.g., I-125), wipe samples should be counted
with a thin crystal NaI scintillation meter.
The net sample count rate is determined by subtracting the background count rate from the
gross count rate.
Sample activity is determined by dividing the net sample count rate by the instrument’s
efficiency for the isotope in question.
Survey results must be documented on a survey log (see Appendix E) or similar form.
Results may be reported as gross count rate, net count rate, or in units of activity (usually
disintegrations per minute). Ensure that the survey log accurately reflects how results are
being reported.
Personnel Dosimetry
The use and type of personnel dosimetry is determined by the activities and functions the
individual performs. By regulation, any person who receives or is likely to receive more than
10 percent of the maximum permissible dose or who enters a high radiation area must be
provided with and must wear personnel monitoring devices.
To obtain dosimetry, complete a Dosimetry Request Form (see Appendix E) and return it to
DRS. Upon receipt, DRS personnel initiate the request process with the dosimetry vendor.
The turnaround time is typically one week for a rush order. Therefore, ensure dosimetry
requests are made in advance of the need to work with radioactive materials. Note that
dosimetry is not issued for individuals working with weak beta-emitting radionuclides such
as H-3, C-14, S-35.
Whole body dosimeters, or badges, monitor exposure to the whole body and should be worn
between the neck and the waist, usually on the front of the body.
Finger ring dosimeters monitor radiation exposure to the hands and fingers. These dosimeters
may be worn on any finger and should normally face the palm side of the hand. Finger rings
must be worn under gloves to prevent them from becoming contaminated.
Every person with assigned dosimetry must wear the dosimetry when working with sources
of ionizing radiation.
The dosimeter reading is the legal record of an individual’s occupational radiation exposure.
Therefore, dosimetry shall be worn only by the individual to whom it is assigned, shall not be
tampered with or experimentally irradiated, and shall not be used to measure radiation
exposure received as a medical patient.
When not being worn, dosimeters must be stored in a location where they will not be
exposed to radiation.
Dosimeters are collected monthly or quarterly by DRS personnel and sent to a vendor for
processing. Dosimeters must be made available for this exchange to occur.
If a dosimeter is lost, discontinue radiation-related activities and contact DRS. Individuals

who have lost their dosimetry must provide information to DRS personnel so that an
assessment of their radiation exposure can be performed. DRS will order a replacement
dosimeter.
Declaration of Pregnancy
The increased sensitivity of rapidly dividing cells makes the human embryo and fetus
particularly susceptible to injury from exposure to ionizing radiation. For this reason,
regulations require that exposure to the fetus during the gestation period not exceed 500
millirem. Recommended reading for pregnant female radiation workers is provided in
Appendix E.
Any radiation worker who is pregnant or believes that she may be pregnant should contact
DRS and review the recommended reading in Appendix E. All inquiries will be confidential.
The individual must complete a Declaration of Pregnancy Form (see Appendix E). If a
written declaration of pregnancy is not submitted, then the worker’s dose continues to be
controlled under the normal dose limits for radiation workers.
For the type of radiation work performed at the U of I, it is rarely necessary to recommend
reassignment or changes to job duties to reduce exposure.
Radioactive Waste Contents Tags Procedure
Radioisotope users are requested to complete waste content tags prior to requesting a pickup
of radioactive waste by DRS. Each bag of dry waste or carboy of liquid waste should have a
tag attached to it.
Instructions on filling out the tags:
Please print legibly and press hard.
LAB SUPERVISOR: Enter the name of the Radiation Permit Holder.
PERMIT NO.: The Radiation Permit Number.
LOCATION: The building and room number where the radioisotope laboratory is located.
PHONE NO.: The Principal Investigator’s office phone number.
DATE SEALED: The date that the container was finally closed after filling.
DRY/LIQUID WASTERADIOACTIVE SHARPS: Indicate whether the waste is in solid,

liquid, or sharps disposal container form. If the waste is liquid waste, specify the volume in
liters. If the waste is in sharps disposal container form, specify the size of the container on
the Cont. # line.
ISOTOPE/ACTIVITY: Indicate the isotope and an estimate of the activity (in mCi). Use
separate lines for multiple isotopes. Activity for liquid organic waste must be determined by
liquid scintillation counting. Activities given for dry waste should be as accurate as possible.
All activities should be decay-corrected if applicable.
BACKGROUND CPM/CONTAINER CPM: The outside of all containers must be

surveyed to ensure that container exteriors are free of removable contamination. Moisten a
piece of filter paper or a cotton swab with water or alcohol. Wipe an area of approximately
100 square centimeters per wipe the outside surface of the bag or container. Record the
background cpm as the count rate from the instrument without radioactive materials present.
Record the container cpm as the net count rate (gross cpm – background cpm). The
container cpm should be less than two times the background count rate. If it is not, either
decontaminate the outside of the bag or place the contaminated bag inside a clean bag and re-
survey.
If the bag contains H-3, C-14, or S-35, swipes must evaluated by be liquid scintillation
counting. Wipes for I-125 should be counted with a NaI detector. Wipes for P-32 should be
counted on a GM detector. Other radionuclides should be counted using appropriate
instrumentation.
SIGNATURE: TAGS MUST BE SIGNED. The signature verifies that all of the information
provided is correct.
DATE: Date that tag was completed.
Attach the completed tag to the container.
After waste has been properly prepared, logon to DRS website at:
http://www.drs.illinois.edu/regwaste/rad/index.aspx
Ensure that laboratory records are properly updated.
NOTE:
DRS reserves the right to refuse to accept any materials that, in the opinion of the staff, have
been improperly prepared or packaged, or if the staff feels that the movement of the materials
would pose an unacceptable hazard to campus personnel or the public.
Records required to be kept in the laboratory
DRS personnel make periodic audits and surveys in radiological laboratories. The following
are expected to be readily available for inspection:
• Laboratory survey records;
• Radioactive material inventory and use records;
• Radioactive waste records (solid and liquid). Sewer disposal records can be kept
either in the laboratory logs or in DRS database.
If the forms in Appendix E are used and maintained, no findings of non-compliance should
occur during DRS audit process. Printouts from automatic counters such as a liquid
scintillation counter may be attached and used as a survey record if the sample numbers
correspond to survey locations. Records should be maintained by the PI for as long as the
radiation permit is active.
DRS personnel perform independent laboratory contamination surveys and audits of

laboratory records. The survey and audit results are sent to the PI via campus mail when
completed and approved. The following two pages are the forms that Division of Research
Safety personnel use to document the results of these surveys and audits.
University of Illinois at Urbana-Champaign
Radiation Safety Section
102 EHSB, 101 S. Gregory St., U MC-225
RADIATION SAFETY SURVEY REPORT
Supervisor: Permit No:

Performed by:
Office:
Survey Date:
Labs
Building Room
Survey Results
Location Direct (cpm) Swipe DPM (per 100 Exposure (mR\h)

cm^2)
Instruments used in this survey:

Instrument:
Instrument:
Instrument:
University of Illinois at Urbana-Champaign
Radiation Safety Section
102 EHSB, 101 S. Gregory St., U MC-225
RADIATION SAFETY AUDIT REPORT

Supervisor: Permit No:
Performed by:
Office:
Audit Dates:
Lab(s):
Status: Satisfactory, Unsatisfactory, Not Applicable, Not Checked

1. Weekly contamination surveys performed when material in use?
2. Are calibrated instruments available for contamination surveys?
3. Are inventory, use and waste records up-to-date?
4. Are there caution signs and employee notices?
5. Do lab workers wear protective clothing, gloves, eyewear, footwear, etc?
6. Is absorbent paper used on the benches?
7. Are training records available for review?
8. Are isotope areas and articles labeled?
9. No mouth pipetting!
10. No eating, drinking and cosmetic use!
11. No improper food storage!
12. Are shielding and handling devices in use?
13. Is the lab locked or attended?
Survey instruments calibrated (mfr., model, SN):

None calibrated
GENERAL LABORATORY SAFETY AUDIT
4. Is radioactive waste stored properly and labeled?

15. Are current emergency posting at the entrance
16. Are Chemical containers labeled properly?
17. Are gas bottles properly secured?
18. Are lab door windows unobstructed?
19. Is housekeeping satisfactory?
20. Are emergency shower/eyewash stations tested?
21. Are emergency/eyewash stations accessible?
Comments:.
Appendix C: Fact Sheets for Commonly Used Isotopes
Isotope Page
Tritium .....................................................................................................................................39
Carbon-14 ................................................................................................................................40
Phosphorus-32..........................................................................................................................41
Phosphorus-33..........................................................................................................................42
Sulphur-35................................................................................................................................43
Chromium-51 ...........................................................................................................................44
Iodine-125 ................................................................................................................................45
Iodine-131 ................................................................................................................................46
Fact Sheets for Commonly Used Isotopes Appendix C
Tritium 3H
Radiological half-life, T1/2……………………………………………………….12.3 years
Principle emission…………………………………………..….18.6 keV beta (maximum)
Dose rate (1 cm from a beta point source)…………………………….300 mrad/h per mCi
Annual limit on intake (ALI) by ingestion……………………………..……..…8x104 μCi
Biological monitoring method………………………….……………………urine samples
Range in air…………………………………………………………………………4.7 mm
Range in water………………………………………………………………..…6x10-3 mm
Shielding required……………………………………………………………………..none
Monitoring method for contamination…………….………wipe survey and LSC analysis
Sanitary sewer release concentration limit…..……………………………....1x10-2 μCi/ml
Special considerations
• Tritium compounds can be absorbed through the skin therefore gloves must always be
worn. Consider wearing two pair of gloves.
• Place previously opened containers of tritiated water into a fume hood, not a
refrigerator. Monitor storage areas where large quantities of H-3 are kept, as certain
forms tend to “creep”.
• After use of >100 mCi on an open bench or >1000mCi in a fume hood, a bioassay by
the Division of Research Safety is required (prior to using H-3, a baseline bioassay is
required)
• Due to its low beta energy, tritium cannot be monitored directly, and therefore regular
wipe surveys of the work areas are recommended.
• ALIs can vary considerably, e.g., DNA precursors such as tritiated thymidine are
regarded as more toxic than tritiated water partly because the activity is concentrated
in the cell nuclei.
Carbon 14C
Radiological half-life, T1/2………………………………………………………5730 years
Principle emission…………………………………………..…...156 keV beta (maximum)
Annual limit on intake (ALI) by ingestion……………….……………..……….2x103 μCi
Biological monitoring method………………………….…………breath or urine samples
Range in air………………………………………………………………………...21.8 cm
Range in water………………………………………………………………..…...0.28 mm
Shielding required………………………………………………………….1 cm plexiglass
Monitoring method for contamination………….....…………………………..GM counter
• Use plexiglass shielding. Do not use lead shielding, which creates Bremsstrahlung
radiation.
• Do not generate carbon dioxide which could be inhaled.
Phosphorus 32P
Radiological half-life, T1/2……………………………………………………….14.3 days
Principle emission…………………………………………..…1.71 MeV beta (maximum)
Biological monitoring method…………………………...…………………..urine samples
Range in air……………………………………………………………………….…..6.1 m
Range in water………………………………………………………………..….….0.8 cm
• Users handling > 10 mCi at a time require a ring (extremity) dosimeter and whole
body dosimeter.
• Use plexiglass shielding. Do not use lead shielding, which creates Bremsstrahlung
radiation.
• Wear eye protection.
Phosphorus 33P
Principle emission……………………………………………0.249 MeV beta (maximum)
Range in air……………………………………………………………………….….49 cm
Range in water………………………………………………………………..….…0.6 mm
Sulphur 35S
Principle emission…………………………………………..…167 keV beta (maximum)
Range in air……………………………………………………………………….….26 cm
Range in water………………………………………………………………..…...0.32 mm
Monitoring method for contamination………….....…….. Swipe survey and LSC analysis
• Surveys for gross levels of contamination may be performed using a Geiger counter.
However, for a more sensitive analysis particularly in radiologically uncontrolled
areas, swipe surveys and LSC analysis should be used.
• Some compounds, such as S-35 methionine, may vaporize upon opening of container.
Therefore, open vials in fume hoods to prevent inhalation.
Chromium 51Cr
Principle emissions………………..……....0.32 MeV gamma (9.8%), 5 keV X-ray (22%)
Exposure rate (1 cm from 1 mCi point source)……………………………………..18 R/h
Biological monitoring method…………………………...……………...whole body count
Half-value layer…………………………………………………………………3 mm lead
Monitoring method for contamination………….………NaI or other scintillation detector
Technetium 99mTc
Radiological half-life, T1/2……………………………………………………….6.02 hours
Principle emission……………………………………………….141 MeV gamma (89.1%)
Dose rate (1 cm from a point source)………………………………….720 mrad/h per mCi
Annual limit on intake (ALI) by ingestion…………………….……………..……….8 mCi
Half value layer………………………………………………………………..…….0.3 mm
Monitoring method for contamination………….....……………………………..NaI probe
Tc-99m is used in clinical and research diagnostic scanning and imaging.
Drying can cause airborne Tc-99m dust contamination, and rapid boiling can cause airborne
Tc-99m aerosol contamination. Expelling Tc-99m solutions through syringe needles and
pipette tips can generate airborne aerosols.
Always wear a lab coat and disposable gloves when handling Tc-99m.
A survey meter equipped with a 1" x 1" or a low-energy NaI scintillation probe is preferred
for the detection of Tc-99m contamination. Typical counting efficiencies: [1" x 1" NaI probe
(39%)] and [low-energy NaI probe (12%-18%)].
Survey meters equipped with a G-M pancake/frisker (15.5 cm2 surface area) can be used;
however, they exhibit very low counting efficiencies (approximately, 1.2%) for detecting
low-energy Tc-99m gamma rays. G-M probes are effective only for gross Tc-99m
contamination.
Indirect counting using a liquid scintillation counter (LSC), gamma counter, or gas
proportional counter (GPC) should be used to detect removable Tc-99m contamination on
smears, swabs, or swipes.
Iodine 125I
Radiological half-life, T1/2………………………………………………………….60 days
Principle emission……………………….35 keV gamma (7%), 27-32 keV X-rays (140%)
Exposure rate (1 cm from 1 mCi point source)……………………………………..1.4 R/h
Annual limit on intake (ALI) by ingestion……………….……………..…………..40 μCi
Biological monitoring method…………………………...……………………thyroid scan
Half-value layer………………………………………………………………0.02 mm lead
• Users handling >1 mCi carrier-free iodine on the open bench or >10 mCi carrier-free
iodine in a fume hood must report to the Division of Research Safety (DRS) for a
thyroid scan within 24-48 hours after use. Prior to work with iodine, a baseline
bioassay must be performed.
• Reduce unbound fractions of carrier-free iodine as soon as possible with sodium

metabisulfate or thiosulfate.
Iodine 131I
Radiological half-life, T1/2………………………………………………………..8.05 days
Principle emission………………………………………………………..364 keV (81.2%)
Exposure rate (1 cm from 1 mCi point source)……………………………………..1.5 R/h
Annual limit on intake (ALI) by ingestion……………….……………..…………..30 μCi
Biological monitoring method…………………………...……………………thyroid scan
Half-value layer……………………………………………………………….0.3 cm lead
• Users handling >1 mCi carrier-free iodine on the open bench or >10 mCi carrier-free
iodine in a fume hood must report to DRS for a thyroid scan within 24-48 hours after
use. Prior to work with iodine, a baseline bioassay must be performed.
• Reduce unbound fractions of carrier-free iodine as soon as possible with sodium

metabisulfate or thiosulfate.
Appendix D: Abbreviations, Conversions, Examples and
Formulas
Abbreviations
ALARA – As Low As Reasonably Achievable

Bq – Becquerel
Ci – Curie
cpm – counts per minute
DRS – Division of Research Safety
dpm – disintegration per minute
GM – Geiger-Mueller
Gy – Gray (unit of absorbed dose)
HPLC –
IEMA – Illinois Emergency Management Agency (formerly Illinois Department of Nuclear
Safety (IDNS))
LDPE – low density poly ethylene
LSC – liquid scintillation count or liquid scintillation counter
mCi – millicurie
NaI – sodium iodide
PI – Principal Investigator
μCi – microcurie
R – Roentgen
Rad – radiation absorbed dose
DRS – Division of Research Safety
Rem – Roentgen equivalent man
Sv – Sievert
Conversions
2.22 x 106 dpm = 1 microcurie

1000 mirocuries = 1 millicurie
1000 millicuries = 1 Curie
Formulas and examples
For determination of meter or wipe survey results, use:
Activity (dpm) = (gross count rate – background count rate)

instrument efficiency
Example: The GM meter response on a benchtop scan was 150 cpm. The
background count rate was 40 cpm. For P-32, the GM efficiency is
Abbreviations, Conversions, Examples, and Formulas Appendix D
approximately 50%. What is the amount of activity on the benchtop?Activity

(dpm) = (150 cpm – 40cpm) = 220 dpm
(0.50)
A survey instrument’s efficiency can be determined for an individual radionuclide using a

known standard (decay-corrected, if necessary) of the radionuclide. The standard is counted
in a fixed geometry and the instrument count rate observed. The efficiency is then
determined by the formula:
Efficiency (%) = (gross count rate – background count rate) x 100

Activity of standard (dpm)
Appendix E: Recommended Forms
Form Page(s)
Radiation Permit Application…………………………………………………………….50-52

Dosimetry Request Form…………………………………………………………………….53
Survey Log…………………………………………………………………………………...54
Radioisotope Use and Waste Log……………………………………………………………55
Declaration of Pregnancy…………………………………………………………………….56
Recommended Reading for Pregnant Female Radiation Workers……………………….57-64
UNIVERSITY OF ILLINOIS at URBANA•CHAMPAIGN
RADIATION PERMIT APPLICATION

Division of Research Safety 101 S. Gregory St., Room 106
Radiation Safety Section Urbana, IL 61801-3070
(217) 244-4559 –or- (217) 244-7233 (217) 333-2755/fax: 244-6594
Applicant Name_____________________________________ Department____________________________

Office Address____________________________________________________________________________
Phone________________ Email__________________@illinois.edu
DRS use only
This permit application is for a(n): New permit. Permit #_____________
Amendment to permit #________
Renewal of permit #_________
List all labs in which you plan to use or store radioactive materials or radiation-producing equipment
and check “Yes” or “No” if these are shared spaces.
Building Room Phone Shared Space
_______________________________________________ __________ ________ Yes No

_______________________________________________ __________ ________ Yes No
_______________________________________________ __________ ________ Yes No
If “YES” has been checked identifying shared space, please list the name of the person(s) who has
responsibility for this shared space.
Name Location
____________________________________ __________________________________________
List the name(s) of those who will be providing the day-to-day operation of the radiation safety program
in the lab.
Name Name
List each radionuclide (of unsealed radioactive material) to be used, the maximum quantity (in
millicuries) that you reasonably expect to possess at any one time, and the chemical/physical form of
each. Note: Once approved, a permit amendment is necessary to increase a radionuclide quantity.
Radiation Permit Application, page 3 of 3 Page 51

University of Illinois Radiation Safety Manual Revision Date: April 2014
Nuclide Chemical/physical form Maximum quantity (mCi)
List each sealed radioactive source and other related information, if any are to be used.
Radionuclide Manufacturer Activity/date Serial number
List all radiation-producing equipment to be used, such as X-ray machines, particle accelerators,
and other equipment capable of producing ionizing radiation.
Type of equipment Model # Types of radiation emitted
Describe any use of radioactive materials in animals. Provide an estimate of the number of animals to
be used, the dosage for each animal, the nature of samples to be taken for measurement, and plans for
disposal of animal extractions and carcasses. (attach additional sheets if necessary)
List all radiation detection instruments available. (attach additional sheets if necessary)
Type of instrument Manufacturer Type of detector (GM, scintillation, ion chamber)
In general, describe the manipulations and handling of radioactive materials to be used in the
laboratory. Include a description of the facilities and equipment that are available at each location
where radioactive materials are to be used. Attach drawings describing the facilities, ventilation (fume
hoods, filtration, etc.), storage facilities, (containers, shielding, etc.), waste receptacles, special
equipment (remote handling tools, etc.), and protective equipment.(attach additional sheets if necessary)
Please submit a description of applicable experience in the use of radioactive materials/radiation-
generating equipment for each individual listed on page 1. Include where the experience was obtained
and the period of experience. (attach additional sheets if necessary)
______
Certification
I certify that the information stated herein is true and correct. This application is made under and in
conformity with all applicable federal, state, and University regulations. I understand that all individuals
working in the areas where radiation hazards may exist, will be informed of: the use and storage of
radioactive materials; the health risks associated with radioactive materials; precautions to minimize
exposure; the responsibility to promptly report any condition which may cause a violation of the
regulations/license or unnecessary exposure to radiation. I further certify that no radioactive material or
radiation-producing equipment will be transferred to another person or place inside or outside of the
University without the prior consent of the Division of Research Safety. Under no circumstances will
radioactive materials be used in humans.
Signature of applicant: Date:
For DRS use only Application checklist
Waste receptacle area Hoods available (if necessary) Sink for liquid disposal
Check lab egress/exits Work areas are clearly marked Radiation detector available
Explain I-number system

Checked by:______________________________ Date:_________________
Radiation Permit Application, page 3 of 3 Page 53

University of Illinois Radiation Safety Manual Revision Date: April 2014
University of Illinois Dosimetry Request Form
Federal, State and University regulations require that your radiation exposure record contain the following
information. Allow 2 weeks for dosimetry to arrive after submitting this for to Radiation Safety. Please complete Part 1
of this form, have your PI complete Part 2, and return the form to:
Division of Research Safety, Radiation Safety Section, MC-225
Part 1………………………………………………………………………………..
(Please print)
Name:________________________________________________ UIN:__________________
last first middle
Date of birth:_______________________ Phone ____________________________________

Email: _______________________________________________________________________
Room/Building where dosimetry will be stored: _____________________________________
Please list below, the radioactive material that you will be working with, the approximate total activities to be used per
month and the time handling the materials during a routine week:
Isotope(s) Quantity (mCi) Handling Time (min/wk)
1. _______________________ ______________ _____________
2. _______________________ ______________ _____________
3. _______________________ ______________ _____________
4. _______________________ ______________ _____________
Xray(s)
1. _______________________ _____________
2. _______________________ _____________
Dosimetry desired (check one or both): Whole Body Badge Extremity Ring
Check one: Sex: M F Ring size (check one): S M L XL
“I am familiar with the radiation hazards of this project and have read or been instructed in the rules and regulations
which pertain thereto.”
Signed:__________________________________________ Date:_____________
Part 2………………………………………………………………………………
“I certify that the above individual’s work may require him/her to be exposed to ionizing radiation and that he/she has
been adequately trained in the procedures necessary to minimize possible hazards.”
Principle Investigator:___________________________________
Signature: _____________________________________________
Date signed:__________ Radiation Permit #______
For Radiation Safety use only
Badge number assigned:___________ Type:________________ Location:_______________

___________ Type:________________ Location:_______________
SURVEY LOG
Supervisor:_________________________________ Location:_______________________________
Detector:_________________ / ________________ Date of Calibration:_______________________

(model) (serial #)
Survey points and results in cpm per area monitored
(points should correspond to locations on survey map)
Back-
Date & Battery Source
ground
Initials check check (cpm) 1 2 3 4 5 6 7 8 9 10
S:/DRS/Forms/Survey Log (rev. 0, 2/2003)
Staple RAM receipt tag here.
Radioisotope Use and Waste Log
Lab Supervisor:_____________________________ Location:______________________

Isotope:_______________________ Vendor:____________________________________
Chemical form:__________________________ Date Received:_____________________
Original Activity:_____________ Assay date:___________ Original volume:_________
Radioisotope Use Record Radioactive Waste Log

Check Sink
Withdrawn Balance Appropriate Box Disposal
Date Initials Date Activity
Liquid Total
Activity Volume Activity Volume Dry
Volume
S:/DRS/Forms/Radioisotope Use & Disposal Log (rev. 0, 2/2003)
DECLARATION OF PREGNANCY
In accordance with the NRC's regulations at 10 CFR 20.1208, "Dose to an Embryo/Fetus," I am declaring that
I am pregnant. I believe I became pregnant in_____________________________________ (only month and
year need be provided).
I understand the radiation dose to my embryo/fetus during my entire pregnancy will not be
allowed to exceed 0.5 rem (5 millisievert) (unless that dose has already been exceeded
between the time of conception and submitting this letter). I also understand that meeting the
lower dose limit may require a change in job or job responsibilities during my pregnancy.
I have been given the opportunity to read USNRC Regulatory Guide 8.13 “Instruction
Concerning Prenatal Radiation Exposure” and IDNS Rules and Regulations, Parts 340.280
and 340.530.
___________________________ ___________________________ ________________

(Your Name Printed) (Your Signature) (Date)
___________________________________________ ____________________
(Work location where dosimetry will be kept) (Phone number)
_________________ _____/_____/_____
(UIN) (Date of birth)
Disclosure Statement
You must provide your name, University ID Number (UIN), and date of birth for the
University of Illinois to process a dosimetry request. Federal and State law require the
University to maintain this information and provide your exposure history upon your
authorization. The University will not disclose a recipient's personal information without the
consent of the recipient to anyone outside the University except as mandated by law.
Complete and return this form via campus mail to:

Radiation Safety, MC-225, 101 S. Gregory St., Urbana, IL,
Division of Research Safety use only:

Fetal badge number assigned:_______ Location:_______ Date issued:______________
S:/DRS/Forms/Declaration of Pregnancy Form (rev. 2, 09/2010)
Recommended Reading for Pregnant Female Radiation Workers
Regulatory Guide 8.13 - Instruction Concerning Prenatal

Radiation Exposure
Revision 3, June 1999
A. INTRODUCTION
The Code of Federal Regulations in 10 CFR Part 19, "Notices, Instructions and Reports to
Workers: Inspection and Investigations," in Section 19.12, "Instructions to Workers,"
requires instruction in "the health protection problems associated with exposure to radiation
and/or radioactive material, in precautions or procedures to minimize exposure, and in the
purposes and functions of protective devices employed." The instructions must be
"commensurate with potential radiological health protection problems present in the work
place."
The Nuclear Regulatory Commission's (NRC's) regulations on radiation protection are

specified in 10 CFR Part 20, "Standards for Protection Against Radiation"; and Section
20.1208, "Dose to an Embryo/Fetus," requires licensees to "ensure that the dose to an
embryo/fetus during the entire pregnancy, due to occupational exposure of a declared
pregnant woman, does not exceed 0.5 rem (5 mSv)." Section 20.1208 also requires licensees
to "make efforts to avoid substantial variation above a uniform monthly exposure rate to a
declared pregnant woman." A declared pregnant woman is defined as a woman who has
voluntarily informed her employer, in writing, of her pregnancy and the estimated date of
conception.
This regulatory guide is intended to provide information to pregnant women, and other
personnel, to help them make decisions regarding radiation exposure during pregnancy. This
Regulatory Guide 8.13 supplements Regulatory Guide 8.29, "Instruction Concerning Risks
from Occupational Radiation Exposure" (Ref. 1), which contains a broad discussion of the
risks from exposure to ionizing radiation.
Other sections of the NRC's regulations also specify requirements for monitoring external
and internal occupational dose to a declared pregnant woman. Licensees are required to
monitor the occupational dose to a declared pregnant woman, using an individual monitoring
device, if it is likely that the declared pregnant woman will receive, from external sources, a
deep dose equivalent in excess of 0.1 rem (1 mSv). The licensee must maintain records of
dose to an embryo/fetus if monitoring was required, and the records of dose to the
embryo/fetus must be kept with the records of dose to the declared pregnant woman. The
declaration of pregnancy must be kept on file, but may be maintained separately from the
dose records. The licensee must retain the required form or record until the Commission
terminates each pertinent license requiring the record.
B. DISCUSSION
As discussed in Regulatory Guide 8.29 (Ref. 1), exposure to any level of radiation is assumed
to carry with it a certain amount of risk. In the absence of scientific certainty regarding the
relationship between low dose exposure and health effects, and as a conservative assumption
for radiation protection purposes, the scientific community generally assumes that any
exposure to ionizing radiation may cause undesirable biological effects and that the
likelihood of these effects increases as the dose increases. At the occupational dose limit for
the whole body of 5 rem (50 mSv) per year, the risk is believed to be very low.
The magnitude of risk of childhood cancer following in utero exposure is uncertain in that
both negative and positive studies have been reported. The data from these studies "are
consistent with a lifetime cancer risk resulting from exposure during gestation which is two
to three times that for the adult" (NCRP Report No. 116, Ref. 2). The NRC has reviewed the
available scientific literature and has concluded that the 0.5 rem (5 mSv) limit specified in 10
CFR 20.1208 provides an adequate margin of protection for the embryo/fetus. This dose
limit reflects the desire to limit the total lifetime risk of leukemia and other cancers
associated with radiation exposure during pregnancy.
In order for a pregnant worker to take advantage of the lower exposure limit and dose
monitoring provisions specified in 10 CFR Part 20, the woman must declare her pregnancy in
writing to the licensee. A separate written declaration should be submitted for each
pregnancy.
C. REGULATORY POSITION
1. Who Should Receive Instruction
Female workers who require training under 10 CFR 19.12 should be provided with the
information contained in this guide. In addition to the information contained in
Regulatory Guide 8.29 (Ref. 1), this information may be included as part of the training
required under 10 CFR 19.12.
2. Providing Instruction
The occupational worker may be given a copy of this guide with its Appendix, an
explanation of the contents of the guide, and an opportunity to ask questions and
request additional information. The information in this guide and Appendix should also
be provided to any worker or supervisor who may be affected by a declaration of
pregnancy or who may have to take some action in response to such a declaration.
Classroom instruction may supplement the written information. If the licensee provides
classroom instruction, the instructor should have some knowledge of the biological
effects of radiation to be able to answer questions that may go beyond the information
provided in this guide. Videotaped presentations may be used for classroom
instruction. Regardless of whether the licensee provides classroom training, the
licensee should give workers the opportunity to ask questions about information
contained in this Regulatory Guide 8.13. The licensee may take credit for instruction
that the worker has received within the past year at other licensed facilities or in other
courses or training.
3. Licensee's Policy on Declared Pregnant Women
The instruction provided should describe the licensee's specific policy on declared
pregnant women, including how those policies may affect a woman's work situation.
In particular, the instruction should include a description of the licensee's policies, if
any, that may affect the declared pregnant woman's work situation after she has filed a
written declaration of pregnancy consistent with 10 CFR 20.1208.
The instruction should also identify who to contact for additional information as well
as identify who should receive the written declaration of pregnancy. The recipient of
the woman's declaration may be identified by name (e.g., John Smith), position (e.g.,
immediate supervisor, the radiation safety officer), or department (e.g., the personnel
department).
4. Duration of Lower Dose Limits for the Embryo/Fetus
The lower dose limit for the embryo/fetus should remain in effect until the woman
withdraws the declaration in writing or the woman is no longer pregnant. If a
declaration of pregnancy is withdrawn, the dose limit for the embryo/fetus would apply
only to the time from the estimated date of conception until the time the declaration is
withdrawn. If the declaration is not withdrawn, the written declaration may be
considered expired one year after submission.
5. Substantial Variations Above a Uniform Monthly Dose Rate
According to 10 CFR 20.1208(b), "The licensee shall make efforts to avoid substantial
variation above a uniform monthly exposure rate to a declared pregnant woman so as
to satisfy the limit in paragraph (a) of this section," that is, 0.5 rem (5 mSv) to the
embryo/fetus. The National Council on Radiation Protection and Measurements
(NCRP) recommends a monthly equivalent dose limit of 0.05 rem (0.5 mSv) to the
embryo/fetus once the pregnancy is known (Ref. 2). In view of the NCRP
recommendation, any monthly dose of less than 0.1 rem (1 mSv) may be considered as
not a substantial variation above a uniform monthly dose rate and as such will not
require licensee justification. However, a monthly dose greater than 0.1 rem (1 mSv)
should be justified by the licensee.
REFERENCES
1. USNRC, "Instruction Concerning Risks from Occupational Radiation Exposure,"
Regulatory Guide 8.29, Revision 1, February 1996.
2. National Council on Radiation Protection and Measurements, Limitation of Exposure to

Ionizing Radiation, NCRP Report No. 116, Bethesda, MD, 1993.
QUESTIONS AND ANSWERS CONCERNING PRENATAL RADIATION EXPOSURE

1. Why am I receiving this information?
The NRC's regulations (in 10 CFR 19.12, "Instructions to Workers") require that licensees
instruct individuals working with licensed radioactive materials in radiation protection as
appropriate for the situation. The instruction below describes information that
occupational workers and their supervisors should know about the radiation exposure of
the embryo/fetus of pregnant women. The regulations allow a pregnant woman to decide
whether she wants to formally declare her pregnancy to take advantage of lower dose
limits for the embryo/fetus. This instruction provides information to help women make an
informed decision whether to declare a pregnancy.
2. If I become pregnant, am I required to declare my pregnancy?
No. The choice whether to declare your pregnancy is completely voluntary. If you
choose to declare your pregnancy, you must do so in writing and a lower radiation dose
limit will apply to your embryo/fetus. If you choose not to declare your pregnancy, you
and your embryo/fetus will continue to be subject to the same radiation dose limits that
apply to other occupational workers.
3. If I declare my pregnancy in writing, what happens?
If you choose to declare your pregnancy in writing, the licensee must take measures to
limit the dose to your embryo/fetus to 0.5 rem (5 millisievert) during the entire
pregnancy. This is one-tenth of the dose that an occupational worker may receive in a
year. If you have already received a dose exceeding 0.5 rem (5 mSv) in the period
between conception and the declaration of your pregnancy, an additional dose of 0.05 rem
(0.5 mSv) is allowed during the remainder of the pregnancy. In addition, 10 CFR
20.1208, "Dose to an Embryo/Fetus," requires licensees to make efforts to avoid
substantial variation above a uniform monthly dose rate so that all the 0.5 rem (5 mSv)
allowed dose does not occur in a short period during the pregnancy.
This may mean that, if you declare your pregnancy, the licensee may not permit you to do
some of your normal job functions if those functions would have allowed you to receive
more than 0.5 rem, and you may not be able to have some emergency response
responsibilities.
4. Why do the regulations have a lower dose limit for the embryo/fetus of a declared
pregnant woman than for a pregnant worker who has not declared?
A lower dose limit for the embryo/fetus of a declared pregnant woman is based on a
consideration of greater sensitivity to radiation of the embryo/fetus and the involuntary
nature of the exposure. Several scientific advisory groups have recommended
(References 1 and 2) that the dose to the embryo/fetus be limited to a fraction of the
occupational dose limit.
5. What are the potentially harmful effects of radiation exposure to my embryo/fetus?
The occurrence and severity of health effects caused by ionizing radiation are dependent
upon the type and total dose of radiation received, as well as the time period over which
the exposure was received. See Regulatory Guide 8.29, "Instruction Concerning Risks
from Occupational Exposure" (Ref. 3), for more information. The main concern is
embryo/fetal susceptibility to the harmful effects of radiation such as cancer.
6. Are there any risks of genetic defects?
Although radiation injury has been induced experimentally in rodents and insects, and in
the experiments was transmitted and became manifest as hereditary disorders in their
offspring, radiation has not been identified as a cause of such effect in humans.
Therefore, the risk of genetic effects attributable to radiation exposure is speculative. For
example, no genetic effects have been documented in any of the Japanese atomic bomb
survivors, their children, or their grandchildren.
7. What if I decide that I do not want any radiation exposure at all during my
pregnancy?
You may ask your employer for a job that does not involve any exposure at all to
occupational radiation dose, but your employer is not obligated to provide you with a job
involving no radiation exposure. Even if you receive no occupational exposure at all,
your embryo/fetus will receive some radiation dose (on average 75 mrem (0.75 mSv))
during your pregnancy from natural background radiation.
The NRC has reviewed the available scientific literature and concluded that the 0.5 rem
(5 mSv) limit provides an adequate margin of protection for the embryo/fetus. This dose
limit reflects the desire to limit the total lifetime risk of leukemia and other cancers. If
this dose limit is exceeded, the total lifetime risk of cancer to the embryo/fetus may
increase incrementally. However, the decision on what level of risk to accept is yours.
More detailed information on potential risk to the embryo/fetus from radiation exposure
can be found in References 2-10.
8. What effect will formally declaring my pregnancy have on my job status?
Only the licensee can tell you what effect a written declaration of pregnancy will have on
your job status. As part of your radiation safety training, the licensee should tell you the
company's policies with respect to the job status of declared pregnant women. In
addition, before you declare your pregnancy, you may want to talk to your supervisor or
your radiation safety officer and ask what a declaration of pregnancy would mean
specifically for you and your job status.
In many cases you can continue in your present job with no change and still meet the
dose limit for the embryo/fetus. For example, most commercial power reactor workers
(approximately 93%) receive, in 12 months, occupational radiation doses that are less
than 0.5 rem (5 mSv) (Ref. 11). The licensee may also consider the likelihood of
increased radiation exposures from accidents and abnormal events before making a
decision to allow you to continue in your present job.
If your current work might cause the dose to your embryo/fetus to exceed 0.5 rem (5
mSv), the licensee has various options. It is possible that the licensee can and will make
a reasonable accommodation that will allow you to continue performing your current job,
for example, by having another qualified employee do a small part of the job that
accounts for some of your radiation exposure.
9. What information must I provide in my written declaration of pregnancy?
You should provide, in writing, your name, a declaration that you are pregnant, the
estimated date of conception (only the month and year need be given), and the date that
you give the letter to the licensee.
10. To declare my pregnancy, do I have to have documented medical proof that I am
pregnant?
NRC regulations do not require that you provide medical proof of your pregnancy.
However, NRC regulations do not preclude the licensee from requesting medical
documentation of your pregnancy, especially if a change in your duties is necessary in
order to comply with the 0.5 rem (5 mSv) dose limit.
11. Can I tell the licensee orally rather than in writing that I am pregnant?
No. The regulations require that the declaration must be in writing.
12. If I have not declared my pregnancy in writing, but the licensee suspects that I am
pregnant, do the lower dose limits apply?
No. The lower dose limits for pregnant women apply only if you have declared your
pregnancy in writing. The United States Supreme Court has ruled (in United Automobile
Workers International Union v. Johnson Controls, Inc., 1991) that "Decisions about the
welfare of future children must be left to the parents who conceive, bear, support, and
raise them rather than to the employers who hire those parents" (Reference 7). The
Supreme Court also ruled that your employer may not restrict you from a specific job
"because of concerns about the next generation." Thus, the lower limits apply only if you
choose to declare your pregnancy in writing.
13. If I am planning to become pregnant but am not yet pregnant and I inform the
licensee of that in writing, do the lower dose limits apply?
No. The requirement for lower limits applies only if you declare in writing that you are
already pregnant.
14. What if I have a miscarriage or find out that I am not pregnant?
If you have declared your pregnancy in writing, you should promptly inform the licensee
in writing that you are no longer pregnant. However, if you have not formally declared
your pregnancy in writing, you need not inform the licensee of your nonpregnant status.
15. How long is the lower dose limit in effect?
The dose to the embryo/fetus must be limited until you withdraw your declaration in
writing or you inform the licensee in writing that you are no longer pregnant. If the
declaration is not withdrawn, the written declaration may be considered expired one year
after submission.
16. If I have declared my pregnancy in writing, can I revoke my declaration of
pregnancy even if I am still pregnant?
Yes, you may. The choice is entirely yours. If you revoke your declaration of pregnancy,
the lower dose limit for the embryo/fetus no longer applies.
17. What if I work under contract at a licensed facility?
The regulations state that you should formally declare your pregnancy to the licensee in
writing. The licensee has the responsibility to limit the dose to the embryo/fetus.
18. Where can I get additional information?
The references to this Appendix contain helpful information, especially Reference 3,
NRC's Regulatory Guide 8.29, "Instruction Concerning Risks from Occupational
Radiation Exposure," for general information on radiation risks. The licensee should be
able to give this document to you.
For information on legal aspects, see Reference 7, "The Rock and the Hard Place: Employer
Liability to Fertile or Pregnant Employees and Their Unborn Children--What Can the
Employer Do?" which is an article in the journal Radiation Protection Management.
You may telephone the NRC Headquarters at (301) 415-7000. Legal questions should be
directed to the Office of the General Counsel, and technical questions should be directed to
the Division of Industrial and Medical Nuclear Safety.
You may also telephone the NRC Regional Offices at the following numbers: Region I,
(610) 337-5000; Region II, (404) 562-4400; Region III, (630) 829-9500; and Region IV,
(817) 860-8100. Legal questions should be directed to the Regional Counsel, and technical
questions should be directed to the Division of Nuclear Materials Safety.
REFERENCES FOR QUESTIONS

1. National Council on Radiation Protection and Measurements, Limitation of Exposure to
Ionizing Radiation, NCRP Report No. 116, Bethesda, MD, 1993.
2. International Commission on Radiological Protection, 1990 Recommendations of the
International Commission on Radiological Protection, ICRP Publication 60, Ann. ICRP
21: No. 1-3, Pergamon Press, Oxford, UK, 1991.
3. USNRC, "Instruction Concerning Risks from Occupational Radiation Exposure,"
Regulatory Guide 8.29, Revision 1, February 1996.(1) (Electronically available at
http://www.nrc.gov/reading-rm/doc-collections/reg-guides/)
4. Committee on the Biological Effects of Ionizing Radiations, National Research Council,
Health Effects of Exposure to Low Levels of Ionizing Radiation (BEIR V), National
Academy Press, Washington, DC, 1990.
5. United Nations Scientific Committee on the Effects of Atomic Radiation, Sources and
Effects of Ionizing Radiation, United Nations, New York, 1993.
6. R. Doll and R. Wakeford, "Risk of Childhood Cancer from Fetal Irradiation," The British
Journal of Radiology, 70, 130-139, 1997.
7. David Wiedis, Donald E. Jose, and Timm O. Phoebe, "The Rock and the Hard
Place: Employer Liability to Fertile or Pregnant Employees and Their Unborn Children-
-What Can the Employer Do?" Radiation Protection Management, 11, 41-49,
January/February 1994.
8. National Council on Radiation Protection and Measurements, Considerations Regarding
the Unintended Radiation Exposure of the Embryo, Fetus, or Nursing Child, NCRP
Commentary No. 9, Bethesda, MD, 1994.
9. National Council on Radiation Protection and Measurements, Risk Estimates for
Radiation Protection, NCRP Report No. 115, Bethesda, MD, 1993.
10. National Radiological Protection Board, Advice on Exposure to Ionising Radiation
During Pregnancy, National Radiological Protection Board, Chilton, Didcot, UK, 1998.
11. M.L. Thomas and D. Hagemeyer, "Occupational Radiation Exposure at Commercial
Nuclear Power Reactors and Other Facilities, 1996," Twenty-Ninth Annual Report,
NUREG-0713, Vol. 18, USNRC, 1998.(2)
ILLINOIS ADMINISTRATIVE CODE

TITLE 32: ENERGY
CHAPTER II: DEPARTMENT OF NUCLEAR SAFETY
SUBCHAPTER b: RADIATION PROTECTION
PART 340, STANDARDS FOR PROTECTION AGAINST RADIATION
Section 340.280 Dose to an Embryo/Fetus
a) Except as otherwise provided in subsections (d) and (e) below, the licensee or registrant
shall ensure that the dose to an embryo/fetus during the entire pregnancy, due to occupational
exposure of a declared pregnant woman, does not exceed 5 mSv (0.5 rem). (For
recordkeeping requirements, see Section 340.1160(d).)
b) The dose to an embryo/fetus shall be taken as the sum of:

1) The deep dose equivalent to the declared pregnant woman during the entire
pregnancy; and
2) The dose to the embryo/fetus from radionuclides in the embryo/fetus and
radionuclides in the declared pregnant woman during the entire pregnancy.
c) The licensee or registrant shall make efforts to avoid substantial variation above a uniform
monthly exposure rate to a declared pregnant woman so as to satisfy the limit in subsection
(a) above.
AGENCY NOTE: The National Council on Radiation Protection and Measurements report
entitled "Recommendations on Limits for Exposure to Ionizing Radiation," NCRP 91,
published June 1, 1987, recommends that no more than 0.5 mSv (0.05 rem) of the allowed
dose to the embryo/fetus be received during any one month during a declared pregnancy.
d) If the declared pregnant woman has not notified the licensee or registrant of the estimated
date of conception, the licensee or registrant shall ensure that the dose to an embryo/fetus, as
specified in subsection (b) above, due to occupational exposure of the declared pregnant
woman does not exceed 0.5 mSv (0.05 rem) per month, during the remainder of the
pregnancy. If after initially declaring her pregnancy, a declared pregnant woman advises the
licensee or registrant of the estimated date of conception, the dose limits specified in
subsections (a) and (e) of this Section shall apply.
AGENCY NOTE: The Department encourages licensees and registrants to explain to

declared pregnant workers that providing an estimated date of conception will enable the
licensee or registrant to more accurately assess the radiation dose to the embryo/fetus and
assist the licensee or registrant in determining appropriate precautions to be taken for the
remainder of the pregnancy.
e) If by the time the woman informs the licensee or registrant of the estimated date of
conception the dose to the embryo/fetus has exceeded 4.5 mSv (0.45 rem), the licensee or
registrant shall be deemed to be in compliance with subsection (a) above if the additional
dose to the embryo/fetus as specified in subsection (b) above does not exceed 0.5 mSv (0.05
rem) during the remainder of the pregnancy.
Section 340.530 Location of Individual Monitoring Devices
Each licensee or registrant shall ensure that individuals who are required to monitor
occupational doses in accordance with Section 340.520(a) wear individual monitoring
devices as follows:
a) An individual monitoring device used for monitoring the dose to the whole body shall be
worn at the unshielded location of the whole body likely to receive the highest exposure.
When a protective apron is worn, the location of the individual monitoring device is typically
at the neck (collar).
b) An individual monitoring device used for monitoring the dose to an embryo/fetus of a

declared pregnant woman, pursuant to Section 340.280(a), shall be located at the waist under
any protective apron being worn by the woman.
c) An individual monitoring device used for monitoring the eye dose equivalent, to
demonstrate compliance with Section 340.210(a)(2)(A), shall be located at the neck (collar),
outside any protective apron being worn by the monitored individual, or at an unshielded
location closer to the eye.
d) An individual monitoring device used for monitoring the dose to the extremities, to
demonstrate compliance with Section 340.210(a) (2)(B), shall be worn on the extremity
likely to receive the highest exposure. Each individual monitoring device shall be oriented to
measure the highest dose to the extremity being monitored.
Appendix F: Glossary
"Absorbed dose" means the energy imparted by ionizing radiation per unit mass of
irradiated material. The units of absorbed dose are the gray (Gy) and the rad.
"Accelerator" (particle accelerator) means any machine capable of accelerating electrons,

protons, deuterons or other charged particles in a vacuum and of discharging the resultant
particulate or other radiation into a medium at energies usually in excess of 1 million electron
volts (MeV).
"Accelerator-produced material" means any material made radioactive by a particle

accelerator.
"Activity" means the rate of disintegration (transformation) or decay of radioactive material.

The units of activity are the becquerel (Bq) and the curie (Ci).
"Adult" means an individual 18 or more years of age.
"Agreement State" means any state with which the U.S. Nuclear Regulatory Commission or
the U.S. Atomic Energy Commission has entered into an effective agreement under
subsection 274b of the Atomic Energy Act of 1954, as amended.
"Airborne radioactive material" means any radioactive material dispersed in the air in the
form of dusts, fumes, particulates, mists, vapors or gases.
"Airborne radioactivity area" means any room, enclosure, or operating area in which
airborne radioactive material, composed wholly or partly of licensed material, exists in
concentrations
(1) In excess of the derived air concentrations (DAC's) specified in Appendix B to 10
CFR 20.1001 - 20.2401, effective January 1, 1998, exclusive of subsequent
amendments or editions; or
(2) To such a degree that an individual present in the area without respiratory protective
equipment could exceed, during the hours an individual is present in a week, an
intake of 0.6 percent of the annual limit on intake (ALI) or 12 DAC-hours.
“ALI or Annual Limit on Intake” means the derived limit for the amount of radioactive
material taken into the body of an adult worker by inhalation or ingestion in a year.
"As Low As Is Reasonably Achievable" (ALARA) means making every reasonable effort
to maintain exposures to radiation as far below the dose limits in 32 Ill. Adm. Code: Chapter
II, Subchapters b and d as is practical, consistent with the purpose for which the licensed or
registered activity is undertaken, and taking into account the state of technology, the
economics of improvements in relation to the state of technology, the economics of
improvements in relation to benefits to the public health and safety and other societal and
Glossary Appendix F
socioeconomic considerations, and in relation to utilization of nuclear energy and licensed or

registered sources of radiation in the public interest.
"Background radiation" means radiation from cosmic sources; naturally occurring

radioactive materials, including radon (except as a decay product of source or special nuclear
material) and global fallout as it exists in the environment from the testing of nuclear
explosive devices. Background radiation does not include radiation from radioactive
materials regulated by the Illinois Department of Nuclear Safety.
"Becquerel" (Bq) means the SI unit of activity. One becquerel (Bq) is equal to 1
disintegration (transformation) per second (dps or tps).
"Bioassay" (radio bioassay) means the determination of kinds, quantities or concentrations

and, in some cases, the locations of radioactive material in the human body, whether by
direct measurement (in vivo counting) or by analysis and evaluation of materials excreted or
removed from the human body.
"Byproduct material" means

(1) any radioactive material (except special nuclear material) yielded in or made
radioactive by exposure to the radiation incident or to the process of producing or
utilizing special nuclear material; and
(2) the tailings or wastes produced by the extraction or concentration of uranium or
thorium from any ore processed primarily for its source material content, including
discrete surface wastes resulting from underground solution extraction processes but
not including underground ore bodies depleted by such solution extraction processes.
"Calendar quarter" means not less than 12 consecutive weeks nor more than 14 consecutive
weeks. The first calendar quarter of each year shall begin in January and subsequent
calendar quarters shall be so arranged such that no day is included in more than one calendar
quarter and no day in any one year is omitted from inclusion within a calendar quarter. No
licensee or registrant shall change the method observed by him for determining calendar
quarters except at the beginning of a year.
"Calibration" means the determination of

(1) the response or reading of an instrument relative to a series of known radiation values
over the range of the instrument; or
(2) the strength of a source of radiation relative to a standard.
"CFR" means Code of Federal Regulations.
"Chelating Agent" means amine polycarboxylic acids (e.g., EDTA, DTPA), hydroxy-
carboxylic acids and polycarboxylic acids (e.g., citric acid, carbolic acid and glucinic acid).
"Committed dose equivalent" (H[T,50]) means the dose equivalent to organs or tissues of
reference (T) that will be received from an intake of radioactive material by an individual
during the 50-year period following the intake.
Glossary Appendix F
"Committed effective dose equivalent" (H[E,50]) means the sum of the products of the
weighting factors applicable to each of the body organs or tissues that are irradiated and the
committed dose equivalent to each of these organs or tissues (H[E,50] = SUM w[T]H[T,50]).
“Critical Organ” means that organ (or tissue) in which the dose equivalent would be the
most significant due to a combination of the organ’s radiosensitivity and a particular dose
pattern throughout the body.
"Curie" means a unit of quantity of radioactivity. One curie (Ci) is that quantity of
radioactive material which decays at the rate of 3.7 x 1010 disintegrations (transformations)
per second (dps or tps).
"Declared pregnant woman" means any woman who has voluntarily informed her
employer, in writing, of her pregnancy.
"Deep dose equivalent" (H[d]) means the dose equivalent at a tissue depth of 1 centimeter
(1,000 milligrams per square centimeter) from external whole-body exposure.
"Depleted uranium" means the source material uranium in which the isotope uranium-235 is
less than 0.711 weight percent of the total uranium present. Depleted uranium does not
include special nuclear material.
"Dose" (radiation dose) means either absorbed dose, dose equivalent, effective dose
equivalent, committed dose equivalent, committed effective dose equivalent, total organ dose
equivalent, or total effective dose equivalent.
"Dose equivalent" (H[T]) means the product of the absorbed dose in tissue, quality factor
and all other necessary modifying factors (e.g., a distribution factor for non-uniform
deposition) at the location of interest. The units of dose equivalent are the sievert (Sv) and
the rem.
"Dose limits" (limits) means the permissible upper bounds of radiation doses established by,
or in accordance with, 32 Ill. Adm. Code: Chapter II, Subchapters b and d.
"Dose rate" means the dose per unit of time, such as rem per minute (rem/min) and millirem
per hour (mrem/hr). See also "Exposure rate"
"Effective dose equivalent" (H[E]) means the sum of the products of the dose equivalent to
each organ or tissue (H[T]) and the weighting factor (W[T]) applicable to each of the body
organs or tissues that are irradiated (H[E] = SUM w[T]H[T]).
"Embryo/fetus" means the developing human organism from conception until the time of
birth.
Glossary Appendix F
"Exposure" means
(1) the quotient of dQ divided by dm where "dQ" is the absolute value of the total charge
of the ions of one sign produced in air when all the electrons (negatrons and
positrons) liberated by photons in a volume element of air having mass "dm" are
completely stopped in air; or
(2) irradiation by ionizing radiation or radioactive material. NOTE: The context makes
clear which is the appropriate definition.
"Exposure rate" means the exposure per unit of time, such as roentgen per minute (R/min)
and milliroentgen per hour (mR/hr). See also "Dose rate".
"External dose" means that portion of the dose equivalent received from any source of
radiation outside the body.
"Extremity" means a hand, elbow, arm below the elbow, foot, knee and leg below the knee.
"Eye dose equivalent" or "lens dose equivalent" means the external dose equivalent to the
lens of the eye at a tissue depth of 0.3 centimeter (300 milligrams per square centimeter).
"Gray" (Gy) is the SI unit of absorbed dose. One gray is equal to an absorbed dose of 1
joule per kilogram (J/kg) (1 Gy = 100 rad).
“Half life, biological” is the time required for the body to eliminate one-half of an
administered dosage of any substance by regular process of elimination.
“Half life, effective” is the time required for a radioactive element in a body to decrease to
one half of its original value as a result of the combined action of radioactive decay and
biological elimination. The effective half life is always shorter than either the radiological or
biological half life.
“Half life, radiological” is the time required for the amount of a particular radionuclide to
decrease to one half of its original value.
"Healing Arts" means the art or science or group of arts or sciences dealing with the
prevention and cure or alleviation of human ailments, diseases or infirmities, and has the
same meaning as "medicine" when the latter term is used in its comprehensive sense.
"High radiation area" means any area, accessible to individuals, in which radiation levels
from radiation sources external to the body could result in an individual receiving a dose
equivalent in excess of 1 mSv (0.1 rem) in 1 hour at 30 centimeters from any source of
radiation or from any surface that the radiation penetrates.
"Human use" means the internal or external administration of radiation or radioactive

materials to human beings.
Glossary Appendix F
"Individual" means any human being.

"Individual monitoring" means the assessment of
(1) Dose equivalent by the use of individual monitoring devices or by the use of survey
data; or
(2) Committed effective dose equivalent by bioassay or by determination of the time-
weighted air concentrations to which an individual has been exposed (i.e., DAC-
hours). (For the definition of DAC-hours, see 32 Ill. Adm. Code 340.30.)
"Individual monitoring devices" (personnel dosimeter or dosimeter) means devices

designed to be worn by a single individual for the assessment of dose equivalent. Examples
of individual monitoring devices are film badges, thermoluminescence dosimeters (TLDs),
optically stimulated luminescence dosimeters (OSLs), pocket ionization chambers, personal
air sampling devices and electronic dosimeters (e.g., silicon diode dosimeters).
"Inspection" means an official examination or observation including, but not limited to,
tests, surveys and monitoring to determine compliance with rules, regulations, orders,
requirements and conditions of the Illinois Department of Nuclear Safety.
"Ionizing Radiation" (see "Radiation")
“Isotope” is a different form of the same chemical element distinguished by having a

different number of neutrons (but the same number of protons) in the nucleus. Nearly
identical chemical properties exist between isotopes of a particular element. Isotope should
not be used as a synonym for nuclide.
"License" means any license issued by the Illinois Emergency Management Agency in
accordance with 32 Ill. Adm. Code: Chapter II, Subchapters b and d.
"Licensed material" means radioactive material received, possessed, used, transferred or

disposed of under a general or specific license issued by the Illinois Department of Nuclear
Safety.
“LSC or Liquid scintillation counting” is a standard laboratory method for measuring

radiation from low energy beta-emitting nuclides. Samples are dissolved or suspended in a
"cocktail" containing an aromatic solvent and small amounts of other additives known as
fluors. Beta particles emitted from the sample transfer energy to the solvent molecules,
which in turn transfer their energy to the fluors; the excited fluor molecules dissipate the
energy by emitting light. In this way, each beta emission (ideally) results in a pulse of light.
The samples are placed in small transparent or translucent (often glass or plastic) vials that
are loaded into an instrument known as a liquid scintillation counter.
"Lost or missing source of radiation" means any licensed or registered source of radiation
whose location is unknown. This definition includes, but is not limited to, radioactive
Glossary Appendix F
material that has been shipped but has not reached its planned destination and whose location
cannot be readily traced in the transportation system.
"Member of the public" means any individual, except an individual who is performing
assigned duties for the licensee or registrant involving exposure to sources of radiation.
"Minor" means an individual less than 18 years of age.
"Monitoring" (radiation monitoring or radiation protection monitoring) means the

measurement of radiation, radioactive material concentrations, surface area activities or
quantities of radioactive material and the use of the results of these measurements to evaluate
potential exposures and doses.
"NORM” or “NARM" means any naturally occurring or accelerator-produced radioactive

material. It does not include byproduct, source or special nuclear material.
"Natural radioactivity" means radioactivity of naturally occurring nuclides.
"Non-ionizing radiation" means radiation that does not produce ionization. Examples are
sound, radio waves, visible, infrared, and ultraviolet light.
"Occupational dose" means the dose received by an individual in the course of employment
in which the individual's assigned duties for the licensee or registrant involve exposure to
sources of radiation. Occupational dose does not include dose received from background
radiation, from any medical administration the individual has received, from exposure to
individuals administered radioactive material and released as authorized by the Illinois
Department of Nuclear Safety, from voluntary participation in medical research programs, or
as a member of the public.
"Package" means the packaging, together with its radioactive contents, as presented for
transport.
"Person" means any individual, corporation, partnership, firm, association, trust, estate,
public or private institution, group, agency, political subdivision of this State, any other State
or political subdivision or agency thereof, and any legal successor, representative, agent, or
agency of the foregoing, other than the U.S. Nuclear Regulatory Commission, or any
successor thereto, and other than federal government agencies licensed by the U.S. Nuclear
Regulatory Commission, or any successor thereto. "Person" also includes a federal entity
(and its contractors) if the federal entity agrees to be regulated by the State or as otherwise
allowed under federal law.
"Personnel monitoring equipment" (see "Individual monitoring devices").
Glossary Appendix F
"Public dose" means the dose received by a member of the public from sources of radiation
from licensed or registered operations. Public dose does not include occupational dose, or
dose received from background radiation, from any medical administration the individual has
received, from exposure to individuals administered radioactive material and released as
authorized by the Illinois Department of Nuclear Safety, or from voluntary participation in
medical research programs.
"Rad" is a unit of absorbed dose. One rad is equal to an absorbed dose of 100 ergs per gram
or 0.01 joule per kilogram (J/kg) (0.01 Gy).
"Radiation" (ionizing radiation) means gamma rays and X-rays, alpha and beta particles,
high-speed electrons, neutrons, protons, and other nuclear particles, or electromagnetic
radiations capable of producing ions directly or indirectly in their passage through matter; but
does not include sound or radio waves, or visible, infrared or ultraviolet light.
"Radiation area" means an area, accessible to individuals, in which radiation levels could
result in an individual receiving a dose equivalent in excess of 0.05 mSv (0.005 rem) in 1
hour at 30 centimeters from the source of radiation or from any surface that the radiation
penetrates.
"Radiation emergency" means the uncontrolled release of radioactive material from a

radiation installation which poses a potential threat to the public health, welfare and safety.
"Radiation Installation" is any location or facility where radiation machines are used or
where radioactive material is produced, transported, stored, disposed or used for any purpose,
except where such radioactive materials or facility are subject to regulation by the Nuclear
Regulatory Commission.
"Radiation machine" means any device that produces radiation when in use, except those
which produce radiation only from radioactive materials.
"Radiation safety officer" means an individual who has the knowledge and responsibility to
apply appropriate radiation protection regulations and has been assigned such responsibility
by the licensee or registrant.
"Radioactive material" means any solid, liquid or gaseous substance, which emits radiation
spontaneously.
"Radioactivity" means the disintegration (transformation) of unstable atomic nuclei by the

emission of radiation.
Glossary Appendix F
"Rem" means the special unit of any of the quantities expressed as dose equivalent. The
dose equivalent in rem is equal to the absorbed dose in rad multiplied by the quality factor (1
rem = 0.01 Sv).
"Restricted area" means any area to which access is limited by the licensee or registrant for
purposes of protecting individuals against undue risks from exposure to sources of radiation.
Restricted area shall not include areas used for residential quarters, but separate rooms in a
residential building may be set apart as a restricted area.
"Roentgen" means the special unit of exposure. One roentgen (R) equals 2.58 x 10-4
coulombs per kilogram (C/kg). (See "Exposure" and Section 310.140 of this Part.)
“Scintillation counter” measures ionizing radiation. The counter consists of a transparent
crystal (such as NaI or Ge), usually phosphor, plastic, or organic liquid (see liquid
scintillation counting) that fluoresces when struck by ionizing radiation. A sensitive
photomultiplier tube (PMT) measures the light from the crystal. The PMT is attached to an
electronic amplifier and other electronic equipment to count and possibly quantify the
amplitude of the signals produced by the photomultiplier.
"Sealed source" means any device containing radioactive material to be used as a source of
radiation which has been constructed in such a manner as to prevent the escape of any
radioactive material.
"Shallow dose equivalent" (H[S]), which applies to the external exposure of the skin or an
extremity, means the dose equivalent at a tissue depth of 0.007 centimeter (7 milligrams per
square centimeter) averaged over an area of 1 square centimeter.
"SI" means the abbreviation for the International System of Units.
"Sievert" (Sv) means the SI unit of any of the quantities expressed as dose equivalent. The
dose equivalent in sievert is equal to the absorbed dose in gray multiplied by the quality
factor (1 Sv = 100 rem).
"Source of radiation" means any radioactive material or any device or equipment emitting,
or capable of producing, radiation.
"Special nuclear material" means

(1) plutonium, uranium 233, uranium enriched in the isotope 233 or in the isotope 235,
and any other material which the Illinois Emergency Management Agency declares
by order to be special nuclear material after the U.S. Nuclear Regulatory
Commission, or any successor thereto, has determined the material to be such, but
does not include source material; or
(2) any material artificially enriched by any of the foregoing, but does not include source
material.
Glossary Appendix F
"Survey" means an evaluation of the radiological conditions and potential hazards incident to
the production, use, transfer, release, disposal, or presence of sources of radiation. Such an
evaluation includes, but is not limited to, measurements or calculations of levels of radiation,
or concentrations or quantities of radioactive material present.
“Thermoluminescent dosimeter or TLD” is a device that measures ionizing radiation

exposure by measuring the amount of visible light emitted from a crystal in the detector
when the crystal is heated. The amount of light emitted is dependent upon the radiation
exposure upon the crystal.
"Total effective dose equivalent" (TEDE) means the sum of the deep dose equivalent for
external exposures and the committed effective dose equivalent for internal exposures.
"Total organ dose equivalent" (TODE) means the sum of the deep dose equivalent and the
committed dose equivalent to the organ receiving the highest dose as described in 32 Ill.
Adm. Code 340.1160(a)(6).
"Unrestricted area" means any area to which access is not controlled by the licensee or
registrant for purposes of protection of individuals from exposure to radiation and radioactive
material, and any area used for residential quarters. NOTE: Licensees or registrants may
control access to certain areas for purposes other than radiation protection, but such action
does not affect whether the areas are unrestricted areas as defined in this Part.
"Very high radiation area" means an area, accessible to individuals, in which radiation
levels from radiation sources external to the body could result in an individual receiving an
absorbed dose in excess of 5 Gy (500 rad) in 1 hour at 1 meter from a source of radiation or
from any surface that the radiation penetrates. NOTE: For very high doses received at high
dose rates, units of absorbed dose (e.g., gray and rad) are appropriate rather than units of dose
equivalent (e.g., sievert and rem).
"Whole body" means, for purposes of external exposure, head, trunk (including male
gonads), arms above the elbow or legs above the knee.
"Worker" means any individual engaged in work under a license or registration issued by
the Department and controlled by a licensee or registrant, but does not include the licensee or
registrant.
"Year" means the period of time beginning in January used to determine compliance with the
provisions of 32 Ill. Adm. Code: Chapter II, Subchapters b and d. The licensee or registrant
may change the starting date of the year used to determine compliance by the licensee or
registrant provided that the decision to make the change is made not later than December 31
of the previous year. If a licensee or registrant changes a year, the licensee or registrant shall
assure that no day is omitted or duplicated in consecutive years.
Index
ALARA, 8, 15, 43, 63 storage, 8
Bioassays, 14-15, 35, 41, 42, 64 use in animals, 9
Containers, 8, 17-20, 29-30 Records, 6, 15, 23, 25-26, 32-33
glassware, 19 Responsibilities,
plastic, 19 Principal investigators/Unit Heads,
sharps, 19 24-25
Declaration of Pregnancy, 13, 31, 53-59 Radiation and Laser Safety
Division of Environmental Health and Committee, 22
Safety, 22, 32, 36 Radiation Safety Officer, 20-21
Dosimetry, 4, 14, 15, 30, 50 Division of Research Safety, 20-21
Emergency Procedures, 10 workers, 25-26
contamination, 10-11 Scintillation, Liquid, 19-20, 27-29, 31-32,
fire or explosion, 10 39-43
injury, 10 Spills, 11, 16, 25, 26
see also Spills intermediate, 11
Exposure, Personnel, 13-15 high-level, 11
minors, 14 Survey, 3, 6, 23, 27-29, 32, 35
non-occupational limits, 13 instrument, 27
occupational limits, 13-14 Log, 51
pregnant workers, 13-14 Procedure, 27-30
records, 15 Training, 4, 16, 24-25
without contamination, 11 Waste, radioactive
see also Bioassays and Dosimetry contents tags, 29
Ionizing Radiation, 2 14, 53 unacceptable disposal, 20-21
see also Permits liquid waste, 20-21, 31
Mixed waste, 23 management, 20-21
Permits, 2 sharps, 18-20, 31
amendments, 2 solid waste, 18-19
application process, 2 see also Scintillation, Liquid and
maintenance of, 2 Mixed Waste
renewal, 2
termination, 3
Radiation and Laser Safety Committee, 1,
3, 15, 18, 24-25
Radiation Safety Officer, 2, 11, 22-25, 68
Radioactive Materials
abandoned materials, 3
off-campus transfers, 7
on-campus transfers, 6
ordering, 5
procurement and transfer, 5
receipt, 6

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University of Illinois

Revised: April 2014

1.0 Introduction ....................................................................................................................... 1

This manual is written primarily for personnel working with beta/gamma-emitting

Appendix A of this manual gives a more detailed description of these responsibilities.

2.1 Radiation Permit Application Process

2.2 Radiation Permit Validity

2.4 Deactivating/Reactivating a Permit

A PI can simply reactivate a previously deactivated permit by contacting DRS. No additional

2.5 Abandoned Radioactive Materials

Situations may arise in which unknown or abandoned radioactive materials and/or

If unknown or abandoned radioactive material or contamination is discovered, DRS will

Particular attention should be given to contamination survey requirements, dosimetry

4.1 Ordering Radioactive Materials

To purchase radioactive materials, the PI submits a completed university purchase requisition

Laboratory personnel must dispose of the shipping material in an appropriate manner. If

4.3 On-campus Transfers of Radioactive Materials

2. Ensure that the material is properly packaged for transport.

4.4 Off-campus Transfers of Radioactive Materials

4.5 Transfers of Radioactive Materials from Off-campus

Occasionally, a PI may receive radioactive material as a gift from another campus or

5.1 Storage of Radioactive Materials

Radioactive gases and volatile forms of radioisotopes should be stored in a well-ventilated

Caution: Radioactive Materials

Labeling is not required if the activity is less than the following:

Nuclide Quantity (μCi)

5.2 Using Radioisotopes in Animals

Ventilation should be adequate to handle the possibility of airborne radioactivity. In some

DRS must approve disposal methods for animal carcasses.

Authorization to administer radioisotopes to animals shall be approved by DRS. DRS

In any radiation emergency, personnel protection comes first, confinement of radioactivity

In an emergency, immediately notify DRS at 3-2755 from university telephones or 217-333-

6.1 Serious Injury and Exposure or Contamination

If someone has received high radiation exposure or radioactive contamination in addition to

6.2 Fire or Explosion in a Radioisotope Area

6.3 High Radiation Exposure Without Contamination

6.4 Intermediate and High-Level Radioactive Spills

In case of a serious accident involving contamination of personnel or equipment (including

7.0 Personnel Exposure

7.1 Occupational Exposure Limits

a. The total effective dose equivalent = 5,000 millirem (0.05 Sv); or

a. Eye dose equivalent = 15,000 millirem (0.15 Sv)

7.2 Non-Occupational Exposure Limits (Members of the Public)

Each user of radioactive material shall conduct operations so that:

7.3 Declared Pregnant Workers Exposure Limits

7.4 Exposure Limits for Minors

7.5 When Dosimetry Is Required

The IEMA requires dosimetry for the following:

Environmental Health and Safety Building

Users of unbound radioactive iodine (typically I-125 or I-131) in quantities of ≥1 mCi on a

Additional bioassays may be required for personnel on a case-by-case basis as determined by

7.7 Personnel Exposure Records

7.8 ALARA (As Low As Reasonably Achievable)

7.9 Exposure Reduction Practices

Table and bench tops should be of a non-porous, chemical-resistant material. Working

8.1 Solid Radioactive Waste Management

As much as possible, wastes shall be segregated according to isotopes. It is especially

No freestanding liquids, lead, sharps or animal carcasses/tissue may be disposed of in solid

8.2 Liquid Scintillation Counting Vials, Glassware, and Plastic Containers

8.3 Radioactive Sharps

8.4 Liquid Waste

Radionuclide Concentration (μCi/ml)

8.5 Animal Carcasses